Chem-Phys1 Flashcards

(703 cards)

1
Q

Scientific Notation

A

method of writing numbers that takes advantage of powers of 10: significand and exponent

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2
Q

Significand

A

absolute value in the rang 1-10, cant be 0

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3
Q

Converting #s to Scientific Notation

A

move the decimal point until the signficand is bigger than or equal to 1 and less than 10

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4
Q

What is 34,600, 0.0003201, 1.10 and 525,600 in scientific notation?

A

34,600, 3201, 1.10, 525,6

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5
Q

When rounding two numbers containing decimals, in which direction should each number for multiplication go?

A

adjust the two decimal points in opposite directions: as one moves up, move the other down

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6
Q

When rounding two numbers containing decimals, in which direction should each number for division go?

A

adjust the two decimal points in the same direction

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7
Q

Scientific Notation Tips

A
  • Count all numbers between the first nonzero digit on the left and the last nonzero digit on the right
  • any 0s to the left of the first nonzero is consider NS
  • 3,490 has 3 sig, 3,490.4 has 4- watch for decimal places
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8
Q

Rounding of Sig Figs

A

round to the number of sig figs that is the same as the least number of sig digits in any of the factors given

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9
Q

X^0 =

A

1

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10
Q

X^A x X ^B =

A

X^(A +B)

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11
Q

X^A/ X^B =

A

X^(A-B)

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12
Q

(X^A)^B =

A

X^ (A x B)

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13
Q

(X/Y)^A =

A

X^A/ Y^A

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14
Q

X^-A

A

1/X^A

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15
Q

X^(A/B)

A

square root with B on the outside of X^A

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16
Q

Perfect Squares Example: square root of 180 =

A

square root of 4 x square root of 9 x square root of 5 = 2 x 3 x square root of 5 = 6 square root 5

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17
Q

square root of 2

A

1.414

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18
Q

square root of 3

A

1.732

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19
Q

LogA 1=

A

0

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20
Q

LogA A=

A

1

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21
Q

Log A x B =

A

Log A + Log B

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22
Q

Log A ^ B

A

BLogA

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23
Q

Log (A/B)

A

Log A - Log B

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24
Q

Log (1/A)

A

-log A

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25
Henderon-Hasselbalch equation
pH= pKa + Log [A-/HA]
26
(a + b) ^2
a^2 + 2ab + b
27
Log (n x 10^m) = log (n) + log(10^m)
= m + log (n)
28
values of sin, cos and tan range
sin and cos range from -1 to 1, tan ranges from - infinity to positive infinity
29
inverse of sin, cos and tan used to find
angle of interest
30
0 degrees sin, cos and tan values
sin = 0, cos = 1, tan = 0
31
30 degrees sin, cos and tan values
1/2, root 3 over 2, root 3 over 3
32
45 degrees sin, cos and tan values
root 2 over 2, root 2 over 2, `
33
60 degrees sin, cos and tan values
root 3 over 2, 1/2, root 3
34
90 degrees sin, cos and tan values
1, 0, undefined
35
180 degrees sin, cos and tan values
0, -1, 0
36
Fahrenheit equation from C
F= 9/5C +32
37
Kelvin equation with C
K= C +273
38
Conversion between metric prexies is accomplished by what?
by muiltpication or divine by appropriate power of 10. For example, millimeters (10^-3) to kilometers (10^3), multiply by 10^-6
39
scientific method
set of steps that defines the appropriate order of event to structure and carry out an experiment
40
scientific method steps
generate testable question, gather data, hypothesis (if-then and testable), collect new data (experimentation or observation), analyze data, interpret data, publish, verify results
41
FINER method
method to determine whether the answer to ones question will dd to the body of science knowledge in practical way and within reasonable period
42
FINER method 5 questions
1. is research study going to be feasible? - obtain necessary supplies, financial or time restraints, gather enough subjects 2. Do other scientists find this question interesting? 3. Is this question novel?-- gain any new knowledge? 4. Would the study obey ethical principles? 5. Is the question relevant outside scientific community?-more important if impact more people
43
errors or biasing during publication are most likely to affect which stages of scientific method?
affect the quality of future experimentation since their is a flawed research base and therefore subsequent hypothesis will be flawed
44
basic science research
experimenter has so much control because done in lab not on people
45
controls
acts as a method of verifying results
46
postitive controls
ensure a change in the DV when it is expected | administer HIV test to HIV positive people
47
negative control
ensure no change in the DV when no change is expected -- placebo effect (observed change when people given a sugar pill) administer HIV test to HIV negative people
48
positive and negative controls create ___
the upper and lower bounds
49
IV
manipulate
50
DV
measure or observe
51
causal relaionships
if the change in the IV always precedes the change in DV< and the change in the DV does not occur in absence of intervention, then causal
52
basic science researcher errors
experimental bias is minimal, except if have faulty hypothesis, failing to publish results that may contradict hypothesis
53
instrument error
may affect accuracy, precision or both
54
accuracy
also called validity- ability of an instrument to measure a true value
55
precision
or reliability - ability of an instrument to read consistently or within a narrow range
56
accurate but not precise
persons weight between 150-190 pounds
57
inaccurate but precise
129 and 131 pounds, but rlly 140 pounds
58
inaccurate tools (but precise) produce
systematic error/bias
59
controls purpose
controls experimental help establish casualty by demonstrating that the outcome does not occur in absence of the intervention. controls are suet keep the manipulation of diff systems as similar as possible, or as known standard against which to judge an experimental manipulation
60
human subjects research
experimental control is low (because of ethics) and relationships are weaker experimental and observational studies
61
randomization
control for differences between subject groups in biomedical research placement of each subject into a control group or treatment group coin toss random
62
blinding
researchers have no information about which group the subject is in
63
single blinded experiments
only the patient or assessor (person who makes measurement on patient) is blinded
64
double blinded experimetns
both investigator, assessor and patient do not know subjects group
65
confounding variables
internal validity decreases, alternative explanations for the data gender, age, lifestyle things, etc
66
types of questions: binary
yes or no, better or worst
67
continuous variables
on a range- percent improvement, weight loss
68
categorical variables
SES, where do you live
69
observational approach
cohort, cross sectional or case -control studies no experiment/manipulation no causality
70
cohort studies
subjects sorted into groups based on differences in risk factors (exposures) and then assessed at various intervals to determine how many subject sin each group had a certain outcome count how many people get lung cancer with 20 people who smoke and 20 people who dont smoke over 40 years
71
cross sectional studies
attempt to categorize patients into different groups at a single point in time prevalence of lung cancer in smokers or nonsmokers at a given point in time
72
case control studies
look at how many subjects have a particular outcome to not, and then look backwards to see how many subjects in each group had exposure to a certain risk factor. 100 patients with lung cancer and 100 people without lung cancer are assessed for smoking hisotry
73
Hill's criteria
observed relationships components that increase the likelihood of causality in the relationship described as correlation for any observational study
74
dose response relationship
as IV increases, increase in response
75
consistency
relationship found in many settings
76
plausiblity
reasonable mechanism for the IV to impact the DV with support by literature
77
specificty
change in DV is only produced by associated change in IV
78
coherence
new data and hypotheses are consistent with the current state of scientific knowledge
79
systematic error bias
does not impact precision, but skews data in one direction or another
80
bias
``` a result of flaws in the data collection systematic error (unidirectional) that occurs when selected subjects or collecting data ```
81
confounding
error during analysis
82
selection bias
subjects used for study are not representative of target population people who volunteer vs. people who dont volunteer gender in study, age
83
detection bias
educated professionals using their knowledge in an inconsistent way. because prior studies indicate there is a correlation, researchers will expect to find one
84
Hawthorne effect
or observation bias, behavior of the study participants us altered because they recognize they are being studied want to look good- exercise more than normal
85
confounding
data analysis error incorrect relationship is characterized third party variables alt explanations
86
causality 3 things
temporal precedence, correlation (associated) and internal vliaidty (no 3rd v)
87
observational relationships
no manipulation of the subjects environment. less conclusive and more subjective than experimental research
88
ethics
beneficence, nonmalefience, autonomy, justice
89
beneficence
obligation to act in the pt best interest
90
nonmalefience
obligation to avoid treatnetrs or intverntions in which harm would outweigh benefits
91
autonomy
responbsity to respect patients decisions and choices about own healthcare
92
justice
responsibility to treat similar patients with similar care, and distribute healthcare fairly
93
Belmont report
respect for persons, justice and benfieince
94
respect for persons
honesty between subjects and researcher informed consent - know al the Risks, benefits, goals to make a knowledgeable decision if want to participant no coercive influence can withdraw consent at any time
95
IRB
protection against unethical studies
96
vulnerable people
prisoners, women and children have special protection with research
97
justice
morally relevant differences - diff between individuals that are ok to treat them differently (age) NOT ok: race, ethnicity, sexual oretination- treat the same important in selection subjects and executing research no harm to any group
98
beneficence
intent to cause a net positive change for both the study population and general population, minimizing potential harms - least invasive, painful or traumatic way catheter or finger poke - equipoise- finger poke Is superior
99
compensatory influence
no impact the decision to participant, coercive influence is which subject loses autonomy to make the decision
100
population
complete group of every individual that satisfies that attributes of interest humans- 7 billion people American F between 18-20 YO
101
parameter
information that is calculated using every person in a population
102
sample
making generalizations about populations based on sample data any group taken from a population that does not include ALL the people random samples!! to ensure represenatative
103
low generalizabilty
narrow conditions for sample selection that do not reflect target population
104
statistically significant
not as a result of random chance
105
internal validity
tendency for same experiment to produce the same results when repeated and provides support for causality
106
external validity
ability to take the info generated and apply it to larger group. also called generalizabilty
107
small sample isses
subject to more random variation than larger samples. if only 1 person is selected, may be an outlier. If larger sample, an outlier has less of an effect on results
108
clinical significance
impact patients - notable change in health status as a result of research intervention
109
protons
found in the nucleus +1 charge atomic number of an element= number of protons (Z) all oxygens have the same amount of protons (8)
110
neutrons
``` neutral, no charge. mass number (A)- sum of the protons and neutrons mass (which makes up most of the atoms mass) a given element can have a variety of neutrons, so have different mass number (same atomic number tho) ```
111
isotopes
atoms with the same atomic number but different mass numbers | determined by neutrons
112
A/Z X
mass number/atomic number Element
113
electrons
-1 charge. very small mass. move around nucleus at varying distances, corresponding to varying levels of electrical potential energy.
114
electrons closer to nucleus have
lower energy levels
115
electrons farther from nucleus (higher electron shells) have
higher energy! strongest interactions with the surrounding environment and weakest interactions with the nucleus. Called valence electrons- more likely to bond with other atoms since dont feel nucleus electrostatic pull. determine reactivity of the atom donating or sharing increases stability in reaching highest energy level
116
positively charged atom
cation
117
negatively charged atom
anion
118
charge is determined by
electrons
119
atomic number is determined by
protons
120
heaviness of an element
atomic weight is constant for a given element, atomic mass or mass number vary from 1 isotope to another (because neutrons)
121
atomic mass
mass of 1 proton= 1 amu= mass of 1 neutron
122
atomic mass of an atom is nearly equal to
its mass number in amu, in sums of protons and neutrons
123
atomic weight
the weighted average of these different isotopes of an element represents both the mass of the average atom of that element in amu and the mass of 1 mole of the element in grams
124
half life corresponds with
stability and proportions of these isotopes
125
a mole is
a number of "things" (atoms, ions, molecules) that equal to Avogadros number (6.02 x 1023)
126
example of atomic weight
atomic weight of C is 12.0 amu, which means that the average carbon atom has a mass of 1 amu and 6/02 x 10^23 C atoms have a combined mass of 12 g.
127
Planck relation
the energy of a quantum E= hf h= Plancks constant = 6.626 x 10^-34 J x s f= frequency of the radiation
128
angular momentum
L=mvr
129
kinetic energy
1/2 m v ^2
130
Bohr Model
angular momentum
131
angular momentum
L = nh/2 pi n= quantum number (+ integer) h=plancks constant (6.626 x 10^-34) angular momentum changes with regards to quantum number
132
energy of the electron equation
E = -(R sub H)/n^2) R sub H = Rydberg unit of energy= 2.18 x 10^-18 J/electron energy of electrons changes with regards to quantum number the energy of the electron increases- becomes less negative- the farther out from the nucleus it is located (increasing n)
133
electrons jump when
the amount of energy exactly is equal to the difference between 1 orbit and another like a staircase, not a ramp
134
the orbit with the smallest, lowest energy radius
ground state (n=1)
135
excited state
when an electron moves to a sub shell of higher than normal energy - an orbit with a larger radii
136
Bohr model importance
explain atomic emission and absorption spear of atoms
137
electrons can be excited with the addition of
heat or energy forms, bu brief and electrons will return to ground state, leading to emission of energy in the form of photons. these energy transition do not form a continuum, but rather are quantized to
138
electromagnetic energy of photons equation
``` E= hc/lambda h= planks constant (6.626 x 10^-34) c= speed of light in a vaccum (3.00 x 10^8 m/s) lambda= wavelength of the radiation ```
139
line spectrum
each line on the emission spectrum (frequency of light) corresponds to a specific electron transition. Because each element can have its electrons excited to a diff set of distinct energy levels, each possess a unique atomic emission spectrum (fingerprint for element)
140
Lyman series
hydrogen emission lines corresponding to transition from energy levels n > 2 to n= 1
141
Balmer series
hydrogen emission lines corresponding to transition from energy levels n >3 to n=2 4 wavelengths in visible region
142
Paschen series
Hydrogen emission lines corresponding to transition from energy levels n >4 to n=3
143
the energy associated with a change in the principal quantum number from a higher initial value ni to lower final value nf is equal to
the emerge of the photon predicted by plancks quantum theory.
144
Combining Bohr and PLancks calucations
E= hc/lambda= R sub H [1/ni^2 - 1/nf^2 the energy of the emitted photon corresponds to the difference in energy between higher energy initial state and the lower energy final state
145
absorption spectrum
when an electron is excited to a higher energy level, it must absorb exactly the right amount of energy to make that transition. energy absorption at a specific wavelength to exciterse electrons of a particular element.
146
each element has a unique
emission spectrum and absorption spectrum (correspond together because the difference in energy between levels remains unchanged ) absorb energy in forms of light and emit in forms of light
147
Bohr's model failed to
explain the structure and behavior of atoms containing more than 1 electron (only did Hydrogen) did not take into account repulsion between many electrons surrounding the nucleus.
148
difference between Bohr's model and modern quantum mechanical model
Bohr thought that electrons followed a clear defined circular pathway or orbit a fixed distance from the nucleus , whereas modern quantum mechanics showed that electrons move more rapidly and are localized within regions of space around the nucleus (orbitals). Impossible to determine where an electron is exactly at any point in time.
149
Heisenberg Uncertanity principle
it is impossible to simulateouly determine, with perfect accuracy, the momentum, and the position of the electon
150
Pauli exclusion principle
no two electrons In a given atom can possess the same set of 4 quantum numbers (n/l/ml and ms)
151
energy state
the position and energy of an electron described by its quantum number. the value of n limits l which limits ml
152
quantum number give info about
size, shape and orientation of the orbitals.
153
quantum number n
principal quantum number. used in Bohr's model and can take on any + integer number. the larger + number, the higher the energy eve and radius of the electron shell.
154
maximum number of electrons within a shell
2n^2 | n- principle quantum number
155
the difference in energy between two shells decreases as the distance from the nucleus increases due to
the energy difference is a function of [1/n^2 - 1/nf^2] ex. difference between n=3 and n=4 shells are 1/9 - 1/16 is less than the difference between n=1 and n=2 shells (1/1- 1/4).
156
azimuthal (angular momentum) quantum number- l
refers to the shape and number of sub shells within a given energy level (shell). important implications with chemical bonding and bond angles.
157
the value of n limits l
for any given value of n, the range of possible values for l is 0 to (n-1). ex. n==2 sub shells l can be 0 or 1.
158
spectroscopic notation
``` principal and azimuthal quantum numbers principal quantum number is a number (1, 2) and l turns into letters l=0: s l= 1: p l=2: d 1=3: f example. n=4 and l=2 =4d ```
159
the energies in the sub shells increase
with increasing l values
160
magnetic quantum number
ml. specifies the particular orbital within a sub shell where an electron is most likely to be found at a given moment in time. each orbital can hold a maximum of 2 electrons. integers between 1 and -1,including 0. s sub shells, with l=0, limits ml to 0 because there is a single value o fm1 and only 1 orbital in s shells. the p sub shell, l=1, ml can be -1, 0 or 1, because there are 3 values for m1 and three values in the p sub shell. d sub shell has 5 orbitals (-2 to +2) and f has seven orbitals (-3 to 3)
161
the shape of the orbital, like the number of orbitals is dependent on
the sub shell in which they are found in: s shells are spheres, p shells are dumbbells
162
as atomic number increases, so does number of electrons
2p contains 3 orbitals. If each orbital contain 2 electrons than 6 electrons can be added during the course of filling 2p orbitals.
163
spin quantum number
ms. spins in +1/2 or -1/2. whenever two electrons are in the same orbital, they have opposite spins- refereed to as paired. electrons in diff orbitals with the same ms values are parallel spins.
164
electron configurations
the pattern by which subshells are filled, number of electrons within each energy level and sub shell is designated by this. use spectroscopic notation, first number denotes energy leveladn the letter is sub shell and subscript is number of electrons in subshell. 2p^4- 4 e- in the second p sub shell of the second energy level (1s and 2s are indicated to be full)
165
Aufbau principle
electrons fill from lower to higher energy sub shells and each sub shell is completed before electrons begin to enter the next one.
166
n+ 1 rule
rank sub shells by increasing energy. the lower the sum of the values of the first and second quantum number, n+ 1, the lower the energy of the sub shells. lower n value, fill with electrons first.
167
Hunds rule
in sub shells that contain more than 1 orbital, such as the 2- sub shell with 3 orbitals. This rule states that within a given sub shell, orbital are filled such that there are a max number of half filled orbitals with parallel spins. Would prefer own orbital before forced to double up with another. due to repulsions. half filled and fully filled orbitals have lower energies and higher stability than other states
168
chromium electron configuraton
Ar 4s^23d^4 but moving 1 e- from 4s to 3d all's 3d to be half filled and be Ar4s^1 3d^5
169
how many electrons each orbital can hold
s- 2 p- 3 d- 10 f-14
170
copper electron configuraton
Ar 4s^13d^10 rather than Ar4s^23d^9 as full d sub shell outweighs the cost of moving an electron out of th 4s sub shell. never observed In p shells- not worth loss of stability.
171
paramagnetic
unpaired electrons in atoms will oreint their spins in a ligament with a magnetic field and the material is weakly attracted to it.
172
diamagnetic
toms that have only paired electrons will be slightly replied by magnetic field
173
valence electrons
outermost energy shells electrons- easily removed and available for bonding
174
IUPAC step 1
identify the longest carbon chain containing the highest-order functional groups, also called the parent chain, If there are two or more chains of equal length, then then the more substituted chain gets priority as the parent chain.
175
IUPAC step 2
number the chain. Number 1 is closest to the highest priority functions group. If all the same priority, numbering the chains should make the numbers of the substituted carbons as low as possible
176
oxidation state
the more oxidized the carbon is, the higher priority it has in the molecule. oxidation state increases with more bonds to the herteroatoms (any atom but H and C) and decreases with more bonds to H.
177
rings- double and triple bonds
everything is the same- numbering from greatest sub. if there is a tie between assigning priority in a molecule with a double and triple bond, double bond takes precendence (not normal)
178
IUPAC step 3
name the subsitutuents. Substituents are functional groups not apart of the parent chain. Name will be placed at the start of the cmpd name as a prefix, followed by name of the longest chain. only the highest priority functional groups will determine the suffix for the cmpd and must be apart of the parent chain.
179
CH3, CH3Ch2, CH3CH2CH2
methyl, ethyl, n-propyl
180
if there are multiple subsitutents of the same type, use these prefixes:
di-,tri-, tetra0, etc.
181
IUPAC step 4
give C number designation and use prefixes | 2,3-dimethyl
182
IUPAC step 5
complete the name. alphabetical order sub!!! prefixes like di-, tri- are ignored when alphabetizing. numbers are separated by commons, and form words with hyphens. example- 4-ethyl-5-isopropyl-3,3-dimethyloctane
183
hydrocarbons
only C's and H's
184
alcohols
C's, H's and OH!
185
alkane
simply hydrocarbons with the formula CnH2n+2. methane- 1C ethane-2C propane-3C butane-4C meth isn't ethical or propiate BUT pent, hex, hept, oct, non, dec, undec, dodec
186
halogens
common sub on alkanes. alkyl halides are indicated by prefix: fluoro, chloro, bromo, iodo
187
-ene, -yne
double and triple bonds. usually is named like a sub and numbered by lowest C. example: 2-butene, or but-2-ene 1,3-butadiene
188
alcohols
named by replacing -e at the end of the name with -ol. -OH gets the lowest possible number, even when there is a multiple bond present due to its higher oxidation state. If alcohol is not highest sub group, then it is called hydroxy-. ex. ethanol 5-methyl-2-heptanol hept-6-en-1-ol
189
alcohols with 2 hydroxyl gross are called diols or glycols
and are indicated with the suffix -diol. ex. ethane-1,2-diol has hydroxy group on each C. diol is added at end.
190
diols with hydroxyl groups on the same carbon
geminal diols
191
diols with hydroxyl groups on adjacent carbons
vicinal diols
192
2-propanol
isopropyl alchol
193
ethanol
ethyl alcohol
194
aldehydes and ketones both contain a
carbonyl group, C=O. with no leaving groups connected to the carbonyl carbon- only connected to the carbon chain or aldehydes with a H. if there is a higher priority group, name ketone and aldehydes with prefix oxo- or keto- for ketones only
195
aldehydes
chain terminating- end of parent chain. generally attached to carbon 1 bc takes priority. Replace -e with -al. ex. butanal
196
ketones
found in the middle of carbon chains. replace -e with -one. give lowest possible number ex. 2-penanone
197
methanal, ethanal, propanal
formaldehyde, acetaldehyde, propionaldehyde.
198
propanone
always ketone on C2. | acetone
199
carbon adjacent to the carbonyl carbon
alpha. successive C's are beta, gamma, and delta. on ketone, both C's are considered alphas in the carbonyl carbon
200
ketones and aldehydes both take precedence over:
alcohols and hydrocarbon chains, and the functional group that is the highest priority determines the suffix. aldehydes usually do suffix because they are terminating
201
carboxylic acids
both a carbonyl group (C=O) and a hydroxyl group (-OH) on a terminal carbon. terminal functional groups like aldehydes. Oxidized carbon!!! (3bonds to it)so HIGHEST PRIORITY GROUP EVER! replace -e with -oic acid.
202
formic acid, acetic acid, propionic acid
methanoic acid, ethahnoic acid, propanoic acid
203
esters
common carboxylic acid dervitaitves. hydroxyl group (-oh) is replaced with an alkoxy group (-OR, where R is a hydrocarbon chain). based on carboxyl naming. first term is how many C are in the hydrocarbon chain ethyl, methyl, propyl, etc. second term is the parent acid, with -oate replacing -oic acid. methyl butanoate
204
amides
carboxylic acid derivative. the hydroxyl group is replaced by an amino group (n containing group). N can be bonded to 0, 1 or 2 alkyl groups (C, H). Suffix is amide. Sub are started with capitol N in front to indicate they are bonded to N- not numbered and prefixed. N-ethyl-N-methylbutanmide
205
anhydrides
carboxylic acid derivative (from 2 actually and water is removed. Cyclic molecules. replace acid with anhydride in the name of the corresponding carb acid if the anhydride is formed from only one type of carb acid. if the anhydride is not symmetrical, both carb acids are named without suffix acid and before anhydride is added. ex. ethnoic propanoic anhydride ethnoic anhydride
206
functional group proriorty list
carb acid (oic acid), anhydride (anhydride), ester (oate), amide (amide), aldehyde (al), ketone (one), alcohol (ol), alkene (ene), alkyne (yne), alkane (ane) suffix ^^^^
207
mendelevs table was arranged by atomic weight, but modern periodic table is arranged by
atomic number (number of protons in an element)
208
A elements
representative elements- groups 1A-VIIIA- valance elcectrons in the orbitals of either s or p sub shells.
209
B elemtns
nonrepresenative elements (transition elements - valence electrons in the s and d subsehlls) and the lanthanide and actinide series (s and f sub shells)
210
metals are
lustrous (shiny), high MP and densities, malleability (can be deformed without breaking), ductility (pulled into wires),low EN, large atomic radius, small ionic radius, low ionization e, low electron affinity, good conductors - two or more osdiations states - loosely held to atoms
211
nonmetals are
upper right side of table. no metallic luster, high ionization energy, electron affinity, EN and small atomic radii and large ionic radii. poor conductors cuz cant give up e-.
212
metalloids
both metals and nonmetals.brittleness but good conductivity.
213
effective nuclear charge
a measure of the net positive charge experienced b the outermost electrons. pull toward the center. increases from L to R of the periodic table . Zeff. constant in given group.
214
principal quantum number
down the elements of a given group, increases. valence electrons are separated from the nucleus.
215
octet rue
tend to be most stable with 8 electrons in valence she
216
atomic radii
equal to 1/2 the distance between centers of 2 atoms in contact with one another. decreases from L to R across a period. atomic radius increases down a group
217
ionic radii
metals lose e- and become +, nonmetals gain e- and become -. metalloids go based on side they fall on. nonmetals close to metalloid line possess a larger ionic radius than counterparts. metals close to metalloid line have more ee- to lose, and experience a less drastic reduction in radius during ionization.
218
ionization energy
energy required to remove an electron from gas/- input of heat- endothermic. high Zeff, more close to nucleus, harder to remove. increases from L to R and bottom to top.
219
electron affinity
energy dissipated by gas species when it gains an electron . opposite of ionization E. exothermic process. the stronger the electrostatic pull (higher Zeff) between the nucleus and valence e-, greater the E release will be when the atom gains an e-. increases across period from L to R, decreases from top to bottom.
220
Electronegativity
measure of thr attractive force that an atom will exert on an electron in chemical bond. greater EN, more it attracts e- within that bond. lower ionization E, lower EN. first 3 nobel gases are exceptions.
221
high reactivity to water
groups 1 and 2
222
six valence electrons
6 and 16 groups
223
contain at least 1 metl
groups 1-15
224
multiple oxidation states
all groups. notably 3-12 (transition metals)
225
- oxidation states
all groups, notably 14-17 (nonmetals)
226
possess a full octet in neutral state
group 18
227
group 1
alkali metals. Zeff low. low densities. low ionization E, low electron affinity, low EN
228
alkaline earth metals
group 2. slightly higher effective muscular charge and slightly smaller atomic radii.
229
active metals
group 1 and 2- so reactive
230
chalcogens
group 16/ eclectic group of nonmetals and metalloids. reactive. 6 e- in valence shell and small atomic radii and large ionic radii. Ozugem
231
halogens
group 17 are highly reactive with 7 e- valence. want to complete octet. gas to solids and liquids. high EN and electron affinity
232
noble gases
group 18. inert gases. limited reactive because 8 valence e-. low BP
233
transition elements
groups 3-12. metals with low electron affinity, low ionization E, low EN, high MP and BP . malleable and good conductors. 'different oxidation states because capable of losing diff #s of electrons from the s and d orbitals.
234
if a newton is the product of a kilogram and m/s, units for pounds are
Force will obey the sam relationship with mass and ace elation, so always m/s. one pound = slightly x ft/secons square
235
smallest to largest
angstrom, cm, inch, foot, mile
236
scalars
numbers that have magnitude only, on direction- distance, speed, energy, pressure and mass
237
A + B and B + A
vectors look the same - no difference in R
238
A- B and B-A
have the same R but in opposite directions
239
scalar is calculated by 2 vectors by using the dot product
A x B = ABcos theta
240
vector is calculated by 2 vectors by using the cross product
A x B = ABsintheta
241
displacement
has magnitude and direction- net change from initial to final direction
242
velocity
rate of change of displacement over time. speed is rate of distance.
243
insanteous speed of an object will always be equal to the magnet of the objects
instaneous velocity, which measures the average velocity as the change in time approached 0
244
average velocity
displacement vector over time- vector
245
average speed
scalar. the rate of total distance traveled over a change time
246
v= d/t
equation
247
total distance traveled can Never be less than the total displacement
because displacement is the most direct route.
248
displacement
velocity over time
249
Equation - gravtional force
``` Fg= Gm1m2/r^2 G= 6.67 x 10^-11 ```
250
friction equation
Friction = muFn
251
Weight equation
Fg= mg
252
acceleration equation
a= v/t
253
direction of the friction force always opposes
movement.
254
if there is no net force acting on an object,
then the objects not expericnign an acceleration and has a constant velocity
255
Force on you by earth and force of you on earth is
equal! forces are reipiorcal in magnitude.
256
Newtons first law
F= ma= 0. A body either at rest or in motion with constant velocity will remain that way unless a net force acts on it
257
Newtons second law
F= ma. An object of mass m will accelerate when the vector sum of the forces results in some nonzero resultant force vector. Accleraiton results from sum of force vectors
258
Newtons third law
Fab= -Fba to every action there is an equal opposite reaction. For every force exerted by A on B, there is an equal but opposite force on B on A
259
equations
``` V= Vo + at x= Vot + at^2/2 V^2= V^2o + 2ax x=vt Fc= mv^2/r ```
260
the only force in free fall and projectile motion
gravity
261
free fall
object falls with constant acceleration, without air resistance. not reach terminal velocity. 9.8
262
projectile motion
2 dimensions, x and y. . objects in motion on earth experience force and accleriton due to gravity only in y axis, Vx remain constant.
263
greattes horizational displacement at angle
sin and cos are at 45
264
greatest vertical displacemnet at angle
launched vertically?
265
translational equilibrium
forces cause objects to move without any rotational. vector sm of all the forces acting on a object is 0, constant speed and direction
266
rotational equlibirium
occurs when forces are applied against an object to cause an object to rotate around a fixed point- torque T= F x r- Frsintheta sum of all torques is 0
267
equation
v= frequency x wavelength
268
period
number of seconds per cycle- T= 1/freq
269
angular frequency
measures in radians per second | = 2 pi frequency or 2pi/T
270
wave speed
is the rate at which a wave transmit the E or matter it is carrying. parodic of frequency and wavlength
271
frequnecy
measure of how often a waveform passes a given point in space. Hz.
272
angular frequency
same as frequency but in radians per second
273
equilibrium position
point with 0 displacement in an oscillating system,
274
amplitude
max displacement of a wave from equilibrium position
275
traveling waves
have nodes and antinodes that move with wave propganda
276
standing waves
defined nodes and antinodes that do not move with wave propgandtion
277
sound waves
longutidal waves
278
principle of supoerposition
when waves interact, the displacemnt of the resultant wave at any point is the sum of the displacement of the two waves interacting together
279
sound is produced by
mechanical vibrations generated by solid objects or fluids. sound is longutidal waves
280
ampltiud oof sound wave is related to its sound level
or volume. frequency of wave is related to its pitch
281
open both sides
wavelength = 2L/n
282
closed on side
wavelength = 4L/n
283
string
wavelength= 2L/n
284
isomers
same moclulear formula, different structures
285
structural isomers
share their molecular formula, meaningg that their molecular weights must be the same different physical and chemical properties different ways to draw C6H14 conformational isomers
286
physical properties
dont change the composition of matter- MP, BP, solubilit, door, color and density
287
chemical properties
reactivity of the molecule with other mc and result in a change in composition
288
stereoisomers
same chemical formula AND same atomic connectivity- same structural backbone. Differ in how these atoms are arranged in space
289
conformational isomers
differentiations in rotation around a single sigma bond. When double bonds hold mc in specific positions, single bonds are free to rotate. Varying degrees of rotation can create different levels of strain
290
conjugational isomers
can be interconverted only by breaking bonds
291
staggered/anti conformation
when 2 big molcules are 180 degrees away from each other and there's no overlap so steric are decreased
292
gauche conformation
from anti to gauche, pass through eclipsed conformation where 2 big groups are 120 degrees apart. when two groups directly overlap with each other (same plane, same side- totally eclipsed)
293
two forms of confirational iosmers
enatioomers and diastereomers
294
chiral
mirror image cannot be superimposed on the OG image-lacks symmetry. looks at hands. chiral center- C- lack a plane of symmetry
295
enatiomers
two molecules that are non superimposale mirror images of one another. same connectivity but opposite configurations at every chiral center in the molecule. have identical physical and chemical properties except topical activity and reactions in chiral environments RS, SR
296
diastereomers
chiral and share the same connectivity, but not mirror images because differ at some chiral centers. occur when a molecule has two or more stereogenic centers and differ at some , but not all of these centers. RR, RS SR, SS SS, RS
297
C atom with 3 different subsitutrants
plane of symmetry and is achiral
298
optical activity
rotation of the plane polarized light by a chiral molecule.
299
racemic mixture
when both positive and negative enantiomers are present in equal concentrations, cancel each other out and no optic activity occurs.
300
cis trans isomera
specific type of diasteromers in which subtituents differ in their position around an immovable bond, like a double bond. Cis if same said, opposite side is trans
301
meso compounds
a molecule with a chiral center that has a plane of symmetry- not optically active
302
Cahn-Ingold-Prelog Priority rules
priority is assigned based not eh atom bonded to the double bonds carbons- higher the atomic number, higher the priority. Used for EZ nomenclature, with double bounds
303
Z
two highest priority sub on each C are not eh same side of the double bond
304
E
opposute sides of the double bond
305
RS
used for chiral (streogenic) centers in mc
306
nomenclature of Chiral
assign priority- right down numbers arrange in space- lowest priority (H) back of mc invert stereochem- any time two groups are switched on a chiral C, the stereochemistry is inverted draw a circle- S= counterclockwise R (to the right)- clockwise
307
fisher projections
horizontal lines indicate bonds that project out front eh plane (wedges) and vertical lines indicate bonds going into the plane (dashes) same steps as above, but after make 1 switch. swap the lowest priority group with one of the groups on the vertical axis. Then turn it 180.
308
ionic bonding
electrons are transferred from 1 atom to another and the resulting ions are held together by electrostatic interactions
309
coavlent bond
electrons are shared between atoms
310
bonding occurs in the
outmost shell of electrons
311
the quantum numbers describe
the shape, size number and origination of atomic orbitals an element posses n--- energy level of a given electron- size. smaller #= closer e is to nucleus and lower its E. L- ranges from 0 to n-1. 0=s 1=p 2=d 3=f ml- orbitals - from -L to +L shape each orbital can hold 2 electrons, which are described by ms: 1/2 and -1/2
312
bonding orbital
if the signs of the wave functions are the same
313
antibonding orbital
If the signs are different a high E (less stable) bond is produced
314
when a molecular orbital formed by head to head or tail to tail overlap
sigma bond! All sigma bonds are single bonds
315
when two p orbitals line up parallel , their electrons clouds overlap
create a pi bond. cannot exist without a sigma bond
316
pi bond to sigma bond
double bond
317
sigma bond and 2 pi bonds
triple bond- hinder rotation
318
the more bonds that are formed between atoms
the shorter the overall bond length is. double bond is shorter than a single bond. Hold atoms more closely together and stronger- require more E to break. although pi bonds individually are weaker to break than sigma bonds- breaking a sigma bond may require more E so double may break to a single. triple bond>double>sims>pi
319
bonding orbitals are more stable than antibonding
so anti has higher E than bonding
320
hybrid orbitals
fome day mixing different types of orbtals
321
how much "s" chatacter
ex. sp^3 | 3 p's and 1 s so 25% s.
322
Carbon is most often bonded with
sp3 hydribitazation
323
sp2
alkenes! 3rd p orbital is left unhydrbizaed and participates in pi bonding. three sp2 orbitals are located 120 degrees apart, separate. two will participate in C-H bonds and the other will do C=C with a sigma bond (with the pi bond above)
324
sp
to form a triple bond, two p orbitals to form pi bonds and third p orbital will combine with s to form two sp orbitals. 180 degrees Can form triple bond or two double bonds in a row like CO2
325
resonace
electrons in molecules that have conjugated bonds- alternating single and multiple bonds- aligns with unhybridized p orbitals down backbone. pi orbitals can delocalize through this p orbital system adding stability to the mc.
326
octet rule
states that an atom tends to bond with other atoms so that it has 8 electrons in its outermost shell
327
incomplete octet
these elements are stable with fewer than 8 electrons in their valence shell and include H (stable with 2), helium (2) , lithium (2) , beryllium (4) and boron (6)
328
expanded octet
any element in period 3 and greater can hold more than 8 electrons, like phosphorous (10), Sulfur (12) chlorine (14)
329
odd numbers of electrons
any molecule with an odd number of valence electrons cannot distribute those e to give 8 to each atom, like NO (11)
330
always do octet rule
O, N, C, F, Na, Mg
331
ionic bonding
one or more electrongs from an atom with low ionization energy, like. a metal, are transferred to an atom with high electron affinity, a nonmetal NaCl electrostatic charges hold groups together crystal lattice structure
332
covalent bonding
electron pair is shared between 2 atoms, nonmetals with similar EN. The degree to which their pair of electrons is shared equally or unequally determines the degree of polarity (dipole) if shared equally- non polar if not- polar
333
cation
atom that loses electrons
334
anion
gains electrons
335
ionic bond
cation and anions, attraction | formed with nonmetal and metal
336
ionic properties
high MP and BP, dissolve in water and polar substances, conductors of Electricity, crysatizze dilative to bring together opposite charge and all away repulsive forces
337
coavlent
when 2 atoms of similar tendery to attract electrons form a compound, energetically favorable then completing a full transfer weak interactions so lower MP and Bp, poor conductors of electricity
338
formation of 1 covalent bond may not be sufficient to fit the valence shell so
atoms form bonds with more than 1 atom single double triple cov bond
339
bond order
number of shared electrons (single =1 , double =2)
340
bond length
average distance between two nuclei of atoms in a bond | as number of shared electrons pair increases, the two atoms are pulled together, decrease in bond
341
bond energy
energu required to break a bond by spectating its component into their isolated gas atomic state- more e- share, more E to break the bond- triple bonds have the greatest energy= stronger bond
342
polarity
differences in EN | dipole
343
non polar covalent bond
no seperation of change across the bond equal or near equation F2, N2
344
polar covalent bonds
uneven sharing
345
non polar cov bonds will form with
En= 0 - 0.5
346
polar cov bonds will form with
En- .5-1.7
347
ionic bonds with form
En- 1.7 or higher
348
strongets to weakest intermolecular forces
H bond> dipole> LDF
349
H bond
H with EN
350
molecule
two or more atoms held together by a covalent bond Co2 - diff elements N2- same element
351
molecular weight
sum of atomic weights for al the atoms in a molecule - amu per molecule
352
formula weight
adding up all the atomic weights of a ion according to empirical formula
353
mol weight of SOcl2
S: 1 x 32.1 amu= 32.1 O: 1 x 16 Cl: 2 x 35.5 = 71 total = 119.1 amu where do u find atomic weights?
354
mole
any substance equal to the number of particiles found in 12 g of c
355
avogadros number (Na)
6.022 x 1023
356
molar mass
mass of one mole of a camped is molar mass : g/mol
357
equvilants
how many moles of the things we are interested in looking at will 1 mole of a given cmpd produce? = mass of cmpd/ gram eqvulant weight gram equiv weight = molar mass/ n
358
law of constant composiiton
any pre sample of a given compound will contain eh same elements in an identical mass ratio water- for every 1 g of H there will be 8 g of O because there is 2 H and 1 O
359
empirical formula
only the ratio and may not give actual number of atoms
360
molecular formula
gives the actual number of atoms of each element in the compound
361
percent composition
mass of elect in form/molar mss x 100
362
combination rxn
two or more rectants form 1 product
363
decomposition Rxn
a singel reactant breaks down into 2 or more products
364
combustion reaction
requires fuel- hydrocarbon and oxygen (oxidant)- produce CO2 and water
365
single displacement rxn
when an atom of ion in a compound is replaced by an atom or ion of another element Cu + AgNO3 --> Ag + CuNO3x
366
double displacement
elements from 2 differ compounds swap places with each other to form 2 new comounds CaCl2 + AgNo3 --> CaNo3 + AgCl
367
neutralization reactions
acid reacts with a base to form a salt and water | a type of double displacemnet reactions
368
limiting reagent
limits amount of product that can be formed int eh reaction
369
percent yield
actual/theoreetical x 100
370
electrolytes
solid ions are poor comducots because the charged particles are rigidly set in place needs to be aqueous solution with ions floating around HCL in water- highly dissociate = high conductors weak electrolyte- ionizes incompletely and only some solute is dissolved- acetic aid, Hg2I2, weak acids, ammonia, weak bases, bipolar gases, glucose, Co2, O2
371
Energy
a systems ability to do work
372
Kinetic energy
energy of motion | k= 1/2 mv^2
373
energy is in
Joules (kg/m^2/s^2)
374
if the speed doubles the kinetic energy will
quadruple
375
potentential energy
given objects position in space
376
gravitational potential energy
PEg= mgh
377
elastic potentil energu
PEel= 1/2 kx^2 k- spring constant - stiffness x- displacement
378
sm of objects potential and kinetic energy= total mechanical energy
E= U + K
379
conservative forces
path independent and that do not dissipate energy- gradational and electrostatic constant mechanical energy remains constant back to initial position - from a to b to a full circle
380
nonconservative forces
decrease mechanical E of system- E is dissipated more E is dissipated with longer path friction, air resistant,
381
work is not a form of eneregyc, but a process by which E is transferred from 1 system to another
other way to transfer is by heat w= F x D work is in J
382
work equations
``` W= Fdcostheta W= P delta V -- isobaric process- pressure is constant W= delta K ```
383
volume stays constant and pressure changes
isochoiric process
384
power
rate at which E is transferred from 1 system t another P= W/t = delta E/t measured in Watt
385
work energy thereoym
Kf- Ki = delt K= W net
386
as the length of the inclined plane increases, the amount of force necessary to perform the same aount o work
decreases (movign the same object the same displacement)
387
the six simple machines are inclined plane
wedge,e wheel and ankle, level , pulley and
388
no heat flows between 2 objects in thermal equilibrium
thermal contact and same temp
389
chemical kinetics
the study of reaction rates the effects of reaction conditions on these rates, mechanisms applied
390
Gibbs free energy
spontaneous and nonspotaneous reactions | whether a reaction will occur by itself or will it need outside assistance
391
rate deterring step
slowest step in any proposed mechanism- acts as a kinetic bottleneck - preventing the overall reaction from proceeding any faster than the slowest step.
392
activation energy
the minimum energy needed for a chemical reaction to occur.
393
collision theory
the rate of a reaction is proportional to the number of collisions per second between the reacting molecules. but not all collisions create a reaction- need to collide with correct origination adn energy to brea old bonds and form new ones. Activation energy barrier needed to be overcome. rate= Z x F z=total number of collisons F- fraction of collisions that are effective
394
arrehenius equation for rate
k= Ae ^(-Ea/RT) ``` k= rate constant A-= frequency T= temp -E= activation energy A= frequency factor ```
395
when molecules collide with energy equal to or greater than teh activation energy they form a
transition state in which old bonds are weakened and the new bonds begin got form. transition state dissociates into products , fully forming the new bonds.
396
delt G reaction
the difference between teh free energy of the produces and the free E of the reactants
397
-delta G
exergonic - energy is given off
398
positive delta G (free energy)
endergonic- energy is absorbed
399
factor affecting reaction rates
greater concentration of reactants- greater number of effective collisions per unit time- increase of frequency factor as temp increases so does reaction rate depends on medium (aqueous , solvents (ethanol) catalysts - increase reaction rate without being consumed- can increase frequency of collisions with reactions, change origination, etc.
400
rate law
rate =k [A]^x [B]^y
401
zero order reaction
rate of formaion of product C is independent of changes in concentration of any of the reactants, A and B constant action rate = to the rate constant k rate = k [A]^0 [B]^0 when temp lowered- rate decreased concentrations doubled- unaffected rate catalyst added- rate increases
402
first order reaction
a rate that is directly proportional to only one reactant , such that doubling the concentration of that reactant results in doubling of the rate of formation of the product. rate - k [A]^1 or rate - k [B]^1 when temp lowered- rate decreased concentrations doubled- rate doubled catalyst added- rate increases
403
second order reactions
rate that is proportional to either the concentration of 2 reacts or to the square of the concentration of a single reactant rate = k [A]^1 [B]^1 rate - k [A]^2 rate - k [B]^2 when temp lowered- rate decreased concentrations doubled- rate multiplied by 4 catalyst added- rate increases
404
carbonyl
in aldehydes and ketones, s well as esters, carboxylic acids, amides, anhydrides double bondbetween a carbon and an oxygen nucleophile or electrophile
405
ketone
2 alkyl groups bonded to the carbonyl | never a terminal group
406
ALDEhyde
1 alkyl group and one hdyrogen bonded to carbonyl terminal group replace the -e at the end of the alkane with the suffix -al. methanols, ethanol, propanal, butanal, pentanal
407
methanol
formadelhyde (1C)
408
ethanol
acetaldehyde (2C)
409
aldehydes as functional groups have prefix
oxo-
410
ketones are named by replacing the
-e with -one two alkyl groups named alphbetcually and then followed yb ketone as subsistuntes, use prefix oxo- or keto- 2-propanone (dimethyl ketone, acetone) 2-butanone (ethylmethylketone)
411
physical properties of aldehydes and ketones
governed by the carbonyl group. dipole is stronger wut carbonyl because double bonded oxygen is more electron withdrawing. increased intermolecular attractions with an elevation in BP (less than alc tho because no H bonding) electrophile- due to electron withdrawing of carbonyl O, partial positive on C. aldehydes more reactive to nucleophiles because have less steric hinderance
412
order of names
meth eth prop but
413
forming an aldelhyde
oxidation of primary alc but can only be produced using weaker oxidizing agents like PCC
414
ketones formed
by the oxidiadation of secondary alcohol
415
nucleophile attack on carbonyl C
nucleophile attacks and forms a covalent bond with the C, breaking pi bond in carbonyl. elections from pi bond are pushed Onto oxygen which accepts extra e- due to electron. Breaking the pi bond forms a tetrahedral intermediate. Need a good leaving group to reform (with aldehydes and ketones- dont reform). Can pick up H from solution and make alc. Good leaving groups are present with carboxylic acid and double bond can reform pushing off the leaving group.
416
geminal diols
in the presence of water . The nuceoleophilic oxygen in water attacks the electrophilic carbonyl Carbonyl C, pushing electrons up from the double bond and attaching water on. Water loses its one H to the top O and so now 2 alcohol
417
aldehydes and ketones treated with alchols
hemiacetal or hemiketal. retention of the hydroxyl group. Attacks (ROH) and oxygen loses double bond. Grabs alcohol H and so there's 1 Alc and 1 OR group. 2 equivalents- proceed to competition with 2 OR groups instead of just 1 (get rid of alc) SN1 reaction OH proontated and lost as water in acidic conditions. form acetals and ketals - protecting groups
418
nitrogen and nitrogen based functional groups act as good
nucleophiles due to teh lone pair of electrons on nitrogen, react radoly with electrophilic Carboxyl on aldehydes and ketones.
419
imine
ammonia adds to the C atom adn water is lost N atom double bonded to to a C atom in Carbonyl - ketones and aldehydes example of condensation reaction because small molecule is lost during formation of a bond between 2 molecules. also a nucleophilic subsection reaction
420
immines and other N groups can undergo tautomeization to form
enamines, which contain both a double bond and a N containing group
421
when HCN (triple bonds and electroneg N atom)reacts with an aldehyde or ketone
cyanohydrin is produced, which is a stable product (C-C bond)
422
oxidation and reduction spectrum
aldehydes are more oxidized than alcohol, but less than carboxylic acids. Ketones are as oxidized as secondary carbons can get.
423
when aldehydes are further oxidized
form carboyxlic acid | with KMnO4, CRO3 Ag2O, H2O2
424
carboxylic acid
r group to a double bond oxygen adn carbonyl C to an alcohol group.
425
hydride reagents
aldehydes and ketones undergo reduction to form alcohol. LiAlH4 and NABH4
426
alpha carbon
adjacent to the carbonyl carbon adn the hydrogens connected to alpha C are termed alpha hydrogens. easy to deprornoate alpha carbon of an aldehyde and ketone because oxygens pulls some electron density away fro the C-H bonds making them weak
427
acidity of alpha hydrogens
by resonance stabilization of the conjugate base and also inductive effects. The electronegative oxygen atom pulls electron density away from C-H bonds, weakening it. Once deprotonaed, resonance stabilization of the neg charge between alpha C , carbon C and electron withdrawing carbonyl oxygen increases the stability of this form
428
the alpha. hydrogens of aldehydes and more acidic than those of
ketones. due to electron donating char of the second alkyl group in ketones. This extra alkyl group destabilizes the carbanion (intermediate with lone pairs instead of H) and disfavors loss of alpha H in ketones compared to aldehydes . Pentanal is stronger acid than pentagon and will have a lower pKA
429
aldehydes are more reactive to nucleus than ketones
due to steric hinderance in ketones- arise from additional alkyl groups that ketones contain (in teh way more so than the aldehyde H) ketones create a higher E intermedate so less likely to proceed
430
enol
C to C double bond and an alcohol. Due to teh acidity of the alpha H, aldehydes and ketones exist in solution as a mixture of 2 isomers- keto and enol form
431
tautomers
the 2 isomers (keto and enology) differe in placement of proton and double bond. Far more keto than enols because thats where equilibrium lies.
432
enoization/tautomerization
interconverting the keto to enroll tautomer.
433
enoate carbanians act as
nucleophiles- Michael addiition | carbanan attacks an alpha beta unsaturation carboxyl compound
434
kinetic enolates
form rapidly and can interconvert with teh thermodynamic form -- favored by fast, irreversible reactions such as with a strong statically hindered base and low temp less stable double bond to the less sub alpha C
435
thermodyanmic enolate
favored by slower reversible reactions with weaker or small bases and higher temperatures
436
enamines
``` tautomers of imines (C=N bond) N may be bound to another alkyl group through tautomerization (movement of a hydrogen nd a double bond) , imines can be converted into enamines ```
437
aldol condensation
generally the same as a nucleophilic addition to a carbonyl , but an aldehyde or ketone acts both as a electrophile (in its keto form) and a nucleophile (in its enolate form) - results in C-C bond.
438
retro adol reaction is the
reverse of an aldol reaction where instead of a bond btween alpha and beta C of a carbonyl , it is broken. This can be favored by the addition of base and heat.
439
aldol condensation Is a ___ reaction
condensation. 2 molecules are joined to form a single moelcule with the loss of a small molecule
440
dehydration rection
molecule of water is lost
441
nucleophile-electrophile reaction
in which a nucleophile pushes an electron pair to form a bond with an electrophile.
442
lewis acid
electron acceptor in the formation of a covalent bond tend to be electrophiles vacant p orbital where they can accept electron pair
443
lewis bse
electron donor in the formaiton of a covalent bond nucleophilies have lone pairs that can be donated- negative charges
444
coordinate covalent bonds
covalent bonds in which both electrons in the bond came from teh same starting atom (Lewis base)
445
bronsted lowry acid and base
acid that can donate a proton | base- accept a proton
446
amphoteric
water- act as bronsted lowry acid and base
447
electrostatics
study of stationary charges and the forces that are created by and which act upon these charges.
448
matter
electrically neutral
449
unit of charge
``` coloumb e = 1.6 x 10-19 C both proton adn electron have this charge, but proton is posotive and electron is negative proton has greater mass electrons greater acceleration ```
450
insulators
will not easily distribute a charge over its surface and will not transfer the charge to another neural object or another insulator. electrons closely linked with nuclei nonmetals glass, hair, water
451
conductors
charges will distribute evenly upon teh surface of the conductor. Able to turner and transport charges and are often used in circuits metals blood, copper, iron
452
coulombs law
Fe = kqq/r^2 | k=9x10^9
453
every electric charge sets up a surrodnign electro field
electric fields exert forces on other charges hat move into the space of the field. E = kQ/r^2 = Fe/q
454
electric field midway meteen 2 negative charges
would be 0 because they are the same charges and cancel out midpoint
455
negaive electrostatic force
points from 1 charge to the other (attaractive)
456
positive electrostatic force
points from 1 charge away from the other (repulsive)
457
direction of the electric field given as teh
direction that a positive test charge would move in teh presence of a source charge. Positive- point outward and negtauve- point inward field lines- used to draw this- closer tg = stronger
458
electric potentil energy
E = kQq/r depends on teh relative position of one charge with respect to another charge if both charges the same (+ and + or - and -) then potential energy will be positive
459
negative charge and positive
unlike charges, more attractive, closer= more stable, negative potential energy
460
2 positive charges
repulsive, potential energy is positive , repel adn therefore closer they are- less stable
461
if both particles have teh same charge
electric potential E decreases as distance increases. if iopposite charges - increases PE as distance increases
462
electrical potential E is Couloumbds law multiplied by
distance
463
Volts = kQ/r
yes
464
electropotential
ratio of a charge's electrical potential energy to the magnutide of the charge itself
465
voltage/potential difference
measure in the change of electric potential between 2 points, which provides an indicator of the tendency toward movement in one direction or the other
466
charg will minimize potential energy
yes
467
equpotential line
potential at every point is the same . sets of points and fdifference between them is the same no voltage or acceleration potential difference
468
electric dipole
separation of charge within a molecule such that there is a permeant or temporary region of equal adn opposite charge at a particular distance V= kd/r^2
469
electric field
need a charge
470
magnetic field
charge that also moves
471
magnetic force
external electric field acting on a charge moving any direction except parallel to the external field
472
condensation reaction
two molecules into one with teh loss of water | carboxylic acids are formed this way
473
carboxylic acids
amides, esters and anhydrides | replace the OH on the carboxyl group with another leaving group
474
amides
RCONR2 formula- just NH replace -oic acid with -amide substituetns on teh nitrogen atom are listed as prefixes and their location is specified with the letter N. synthesized with carboxylic acids adn ammonia/amide loss of H from the nucleophile ex. N,N-dimethylethanamide
475
cyclic amides
lactans | beta- bond between b carbon and teh nitrogen
476
ester
dehydration synthesis products of other carboxylic acid derivatives and alcoholics esterifying group(sub bonded to O) as a prefix -oate relates -oic acid ethyl ethanoate triglycerides - storage form of fats in the body: esters of long chain carboxylic acids
477
cyclic esters
lactones
478
sponification
the process by which fats are hydrolyzed under basic conditions to produce soap
479
anhydrides
condensation of dimers of carboxylic acids RC(O)OC(O)R symmetrical anhydrides- name acid instead of anhydride at end (ortho-phthalic acid) formed y heating carboxylic acids and driven forward by increased stability of newly formed rings (5 or 6 ring) high BP alcohols can act as nuc to anhydrides to form esters and carboxylic acids anhydrides can be reverted back to caroboxylic acid by exposing them to water
480
steric hinderance
describes when a reaction doe snot proceed due to teh size of the sub affect ability of the nuc to access the carbonyl carbon thus affects reactivity
481
induction
distortion of charge across sigma bonds dipole electrons attracted to atoms that are more electroneg, generating a dipole carboxylic acids groups to nuceophooc attacks
482
carboxylic reactive groups
anhydride, esters, amides anhydrides are stable with resonance and electron withdrawing O is very electrophilic amides- electrons donating amino group
483
conjugation
presence of alternating single and multile bonds
484
lactams and lactones are more reactive to hydrolysis because they
contain more strain | torsional strain from eclipsing interaction and angle strain from compressing sp3 angle
485
in the formation of amide from ammonia and an anhydrde
nucleophile - ammonia electrophile- one of the carbonyl C of the anhydride alc also nuclei to anhydrides
486
tranesterifcation
exchange of one esterfying group for another in an ester reaction requires an alchol as a nucleus ethyl group of the alc replace the isopropyl butonate
487
strongly acidic conditions catalyze amide hydrolysis by
protonating the oxygen in teh carbonyl | increases the electrophilcity of the Carbon, making it more susceptible to nuclear attacks
488
snucleophilic acyl substation attack of teh carbonyl carbon results in the
displacement of a LG formation of amides from nuc sub reactions between ammonia and any carboxylic acid- - also a cleavage reaction because splits anhydride
489
strongly basic conditions catalyze amide hydrolysis by
increasing the concentration of -OH, which can act as a nuc on amide carbonyl
490
amino acids
contain an amino group (NH2) and a carboxyl group attached to a single carbon atom (alpha C) other 2 sub are a H atom and a R group alpha C is chiral (stereogenic center) besides for glycine because r group is H
491
amino acids are chiral so they are
optically active and L isomers | have S configuration except for cusstein which is R
492
amino acid characteristics
acidic carboxyl group and basic amino group are amphoteric molecules act as both acid and bases! amino groups can take on positive charge by being protonated and carboxyl groups can take on negative charge when deprotonated.
493
when an amino acid is put in positive and negative charges
take on both and form a zwitterion
494
amono acids are grouped into 5 categoties
non polar aromatic, aromatic, polar, negatively charged (acidic) and positively charged (basic)
495
non polar aromatic
side chains saturated by hydrocarbons like alanine, valine, leucine, isoleucine and also glycine and proline and met
496
aromatic amino acids
tryptophan, phenylalamine, tyrosine
497
nonpolar amino acids
hydrophobic can be aromatic or not interior or proteins
498
polar amino acid
terminal groups containing oxygen, N, sulfur- serine, threonine, asp , glutamic, cysteine
499
negtaively charged amino acids
aspartic acid and glutameric acid terminal carboxylate anions in their R groups
500
positively charged amino group
arg, lysine, his have a protonated amino group in their R groups
501
polar acidic and basic amino acids are all
hydrophilic and tend to form H bonds with water
502
amino acids undergo condensation reactions to form
``` peptide bonds (through polypeptides) are the base unit of proteins hydrolysis of pteptide bonds is catalyzed by a strong acid or base ```
503
C-N bond of an amide is
planar because it has a double bond characteristic due to resonance. Double bonds exist in a planar configuration and restrict movement.
504
stecker synthesis
one starts with an aldehde, ammonium chloride and potassium cycanide. Carbonyl oxygen is protonated, increasing electrophilicty of teh carbonyl carbon. Ammonia attack carbonyl C to form an immine which is susceptible for a nuc attack and CN- anion from KCN attacks forming Nitrile group (-C triple bond to N) final molecule is a aminonitrile- NH2 (amino group) and a nitrile group. water used to hydrolyze aminonitrile to form the amino acid a condensation reaction (formation of imine from a carbonyl containing cmpd and ammonia with loss of water) followed by nuc addition(adition of nitrile group) followed by hydrolysis
505
Gabriel Synthesis
proceeds through 2 SN2 reactions, hydrolysis and decarboxylation begins with potassium phthalimide and diethyl bromomalonate , followed by an alkyl halide. Water is then used to hydrolyze the resulting cmpd to form teh amino acid. acid and bases as catalyst.
506
phosphoric acid
forms the high energy bonds that carry E in ATP inrognaic phosphate or phosphate group AKA ha a very negative charge. when bonded to other phosphate groups in a nucleotide triphosphate, this creates repulsion with adjacent phosphate groups , increases E of the bond can be resonance stabeized
507
organic phosophates
C containing molecules with phosphate groups like DNA, ATP, GTP
508
the 3 H in phosphoric acid have very different pkA values - allows phosphoric acid to
pick up or give off protons in wide pH range/ good buffer
509
extraction
the transfer of dissolved compound (desired product) from a starting solution into a solvent in which the product is more soluble like dissolves like- polarity step 1: 2 solvents are immiscible (2 layers that do not mix), different polarities or basic base properties so that a compound of interest ins dissolve more easily In one than the other repertory funnel - denser layers sink to the bottom (organic layer on top) and drain inorganic from the bottom. Keep adding teh solute (water), shake, settle, exact - multiple extractions is best desire product + water- rotary evaporator evaporates water
510
acid and bases
dissovle more easily in opposite acid base char. ex. acid dissolves more easily in base as it creates a conjugate base and highly charged (soluable)
511
distillation
takes advanatge of BP in order to seperate solutions of miscible liquids by evaporation adn condensation lower BP- vaporize first - condenses as liquid and drips down into a vessel (distillate). heating temp kept low so that the liquid with teh high BP will nt be able to make it distillate container
512
filtration
isolates a solid from a liquid | residue (left behind-solid) adn filtrate (liquid)
513
recrystallization
further purifying crystals in solution dissolve product in hot solvent and let it recrystaize as it cools - desired product will recrysalize at this specifi chigh temp and imurities will remain liquid
514
simple distillation
described above. | between temp 150 C and 25 C
515
vaccum distillation
distil a liquid with a BP over 150 C vaccumn lowers ambient pressure, decreasing the temp that the liquid must reach in order to have a good vapor pressure to boil can distill compoudsn with high BP at lower temp
516
fractional distilzation 1
seperate 2 lipid with similar BP (less than 25 degrees apart_
517
chromatogaphy
key: more similar a compound is to its surroudnings (polar, charge, ) more it will stick to and move slowly through its surroundings
518
ion exchange chromatgraphy
the column is given a charge, which attarcts molecules with teh opposite charge
519
size exclusionc hromatgraphy
small pores are used- smaller moleucles are trapped while larger molecules pass through teh column
520
affinity chromatography
spceific receptors or antibodies can trap the target of teh column; target must then be washed out using other solutons
521
gas chromatography
mpbiel and sationary phase with gas instead of liquid stationary - metal (where the sample is placed) ad then it is run through a stationary phase (liquid or gas) and will displace or elute teh sample adn will adhere to the stationary phase at differing strengths substances migrate at different speeds- isolate them (partionining)
522
mass spec
molecular eight determination: ionization and fragmentation of compounds in an magnetic field and separates based on mass to charge ratio
523
high performance liquid chromatography
HPLC.used to be with high pressure but now performed with a solvent and temp gradients, specific separation
524
carboylic acids
nucleophiles, electrophiles, acids (give away protons) very stable and acidic hydrogen bnding - so High BP an intermolecular forces -oic acid highest priority functional group
525
cyclic carboxylic acids
suffix carboxylic aci
526
carboxylic acid properties
simila to aldehydes and ketones but another acidic H to participate in runs and hydrogen bond polar- contain carbonyl group hydrogen bond bc contain H bonded to electroneg hydroxyl O form dimers because of high intermolecular attraction- connected via hydrogen bond acidic so negative charge haev a stable conjugate base, easier for proton to leave, stonger acid
527
electron withdrawing sub makes the anion
more syable and therefore increase acidity electron donating sub destabilize the anion and casue the carboxylic acid to be less acidic- closer sub us to carboxylic acid, stronger effect
528
photoelectric effect
when light with a sufficient high frequency is incident on a metal on a vacuum, the metal atoms emit electrons, producing a net charge (current)
529
light beams of greater intensity produce
a larger current , larger electrons liberated from the metal
530
when the lights frequency is above the threshold frequency, the magnitude of the resulting current is directly proportional to
the intensity (amplitude) of the light beam
531
threshold freqency
minmum frequency to cause ejection of electrons. depends on type of metal. all or none response. if less than threshold, no response
532
Photons
light quanta
533
energy of photons equation
E= hf E- energy of photon go light h- planks constants (6.626 x10^-34) f- frequency of light
534
wavelength and frequency equation
c = wavelength x frequency c- speed of light - 3 x 10^ 8 waves with higher frequency have shorter wavelengths
535
when electrons are ejected, excess energy is connected to kinetic energy
Kmax = hf-W | W- work
536
work
minimum energy required to eject an electrtron. any excess turns into kinetic e W= hf(t f(t)- threshold freqneyc
537
Bohr model of an atom | atomic absorption
electron energy levels are stable and discrete, corresponding to specific orbits. An electron can jump from a lower E state to a higher E state by absorbing a photon of light of right frequency to match teh difference between orbits (E= hf)
538
when an electron falls from higher E state to lower E state
emits photon with energy equal to teh energy difference between 2 orbits atomic emission
539
IV spectra
used to find chemical structure because different bonds will absorb different wavelengths of light
540
UV vis spec
looks at absorption of light in teh visible and UV range.
541
change in molecular structure can cause shifts in absorption patterens
acid state- clear basic state - bright pink- absorb all bu the longer wavelengths of visible light can be protonated or deprotonated, double bond or aromatic
542
fluroence
excites with UV radiation, glow with visible light. Photons of UV light have high freuqnwcy (shorter waveengths). after being excited to a higher state by UV, electron in the fluorescent substance returns to its OG state and involves less energy as it goes down- photon is emitted with a lower frequencyy the UV. if within the visible range, glow
543
energ ydifference between ground state e and higher level e determines
the frequency of light a particualr material absorobs (absorption spectra)
544
mass defect
``` the mass of the nucleus is slighter smaller than just addign protons and neutrons. E = mc^2 E= energy m- mass c- speed of light ``` result of matter beign converted to energy (binding energy). have a strong nuclear force, attacrt neutrons and protons together evenn tho repulsive.
545
fourfundamental forces of nature
strong and weak nuclear forces | electrostatic forces, gravitation
546
mass defect adn biding e
transformation of nuclear mass to E with a resultant loss of matter E= mc ^2
547
nuclear reactions
fusion, fission and radioactive decay- combing or splitting of nuclei of atoms intermediate sized atoms are most stable, when small atoms combine or large atoms split there is a lot of E released.
548
isotopic notation
elements are preceded by tehir atomic number as a subscript and mass number as a superscript A - mass number- protons plus neutrons X Z- atomic number- number of protons
549
fusion
small nuclei combine to form larger nucleus | (hydrogen helium) - increase in nuclear mass during rection
550
fission
large nucleus splits into smaller nuclei. | (actinides, lanthanides)- decrease in nuclear mass during a reaction
551
radioactive decay
spontenous decay of certain nuclei accompanioned by the emission of specific particles
552
isoltop decay
X (parent nucleuse) goes through nuclear delay to form Y (daughter nucleus) + emitted decay particle mass numbers and Tomic numbers must be the same on both sides of the equation- balance!
553
alpha decay
emission of alpha paticle massive cmpared to the beta particle, double the charge emission of alpha particle means that the atomic number of the daughter nuc will be 2 less than that of parent and parent number will be 4 less. -4- A X (alpha) (He) -2- Z
554
beta decay
emission of beta particle, or an electron. when a neutron decays into a proton. rlly penetrating that alpha radiation positron- mass of e but + charge emitted: z = -1 (so add one to Z of parent) adn A=0-- may emit antineutrino opposite when protn to neuron (+1 so minus 1 to Z) may emitneutrino in beta positive
555
gamma decay
gamma rays emitted, which are high energy / high frequency photons. carry no charge and simply lower the E of the parent nucleus without changing mass or atomic number.
556
electron capture
capture an inner electron that combines with a proton to forma neutron. Atomic Number is -1 (Z) than the original. reverse of beta decay absorbs e-
557
half life
time it takes for half of the sample to decay
558
gamma radiation produces electromagnetic radtion
rather than nuclear fragments, it can be detected on an atomic absorption spectra.
559
reactions that involve the transfer of electrons from one chemical species to another
oxidation reduction (redox) reactions
560
oxidation
loss of electrongs
561
reduction
gain of electrons
562
oxidzing agent
causes another atom in a redox reaction to undergo oxidation and itself its reduced
563
reducing agent`
causes the other atom to be reduced and it self is oxidized.
564
OIL RIG
oxidation I sloss, reduction is gain
565
almost all oxiizing agents contain oxygen or another EN element
like a halogen O2, H2So4 KMnO4 +
566
reducing agents
contain metal ions or hydrides (H-) CO, C, B2H6 NADH
567
alcohols
ROH -OH funcitonal group is hydroxyl replace -e with -ol if highest priority, alcohol receive lowest possible number. If not, named as subsitutient with hydroxy- prefix
568
phenols
``` alcohol rings hydroxyl Hydrogens are rlly acidic due to resonance within the phenol ring w groups on adjacent C- ortho seperate C- meta opposite sides of ring- para ```
569
physical properties of alc
``` hydrogen bonding (H attached to EN molecules like O, N, F) as a reuslt of extreme polarity higher MP and BP ```
570
hydroxyl H of phenols are more acidic tha those of other
alchols- due to teh aromatic nature of the ring and resonance stabilization of the negative charge on O
571
alcohols with highest BP
more hydroxyl moleucles, more H bonding | long chain has increased LDF forces ad therefore lower BP
572
electron withdrawin sub
increase acidity as electron donating groups decrease it
573
oxidation of primary alc to aldehydes
PCC. stops here bc PCC lacks the water necessary to hydrate the otherwise easily hydrated aldehyde with other oxidizing agents, aldehydes are rapidly hydrated to form geminal diols (1,1-diols) which for carboxylic acids after oxidized again
574
secondary alc can be oxidized to ketones by
PCC or any stonger oxidizing agent
575
tertiary alc cannot be oxidized becasue they are already as oxides as they can be
without breaking a C-C bond
576
oxidation of primary alc with chromium VI (Na2Cr2O7 and K2Cr2O7) will produce
carboxylic acid and secondary alcohol to ketones
577
CrO3- Jones oxidation
oxidizing primary alc to carboxylic acids and secondary alc to ketones
578
hydroxyl groups are poor LG of
nuc sub reactions if protonated or reacted with to form better LG mesylate is a compound containing the functional group -SO3Ch3 Teslates: -So3C6H4Ch3- forming ester also help with protecting groups
579
aldehydes or ketones can be reacted with 2 equvi of alcohol or diol to form
acetal or ketal- less reactive than aldehydes and ketones and thus proetct the functional group from reacting
580
treatment of penols with oxidizing agents
produce quinones resonance stabilized electrophiles sometimes aromatic
581
DKA
diabetic ketoacidosis can arise from th result of the bodies metabolism of FA when insulin production shut down. FA are then metabolized into ketone bodies as an alt E source to glucose, some ketones producted are ketone acids and
582
irreversiable
reaction proceeds in 1 direction | determined by the Rate limiting reagent
583
reversible
forward or reverse do not usually proceed through completion because products can react to form Reagan's forward= reverse
584
dyanmic equilibrium
forward and reverse reactions ae occuring
585
static equilbium
going a the same rate reactions in forward and back so no change in the concentration of the products or reagents
586
entropy
measure of the distribution E throughout a system or between a system and its environment
587
law of mass action
Keq= {C^C][D^D]/[A^A][B^b} | is the system is at equilbiurm
588
reaction quotient Q
same equation as K, but measures concentrations at any point in time QKeq froward reaction has succeeded and reagents are lower concentration
589
Q and Keq
Q< Keq: forward reaction has not yet reached equilibrium greater concentration of reactants Q= keq: dynamic equilibrium and forward and reverse are equal Q> Keq: forward reaction exceed equilibrium and product is more
590
the concentrations of pure liquids and l=solids do not appear
in teh equilibrium expression because based on activities of compounds not concentrations
591
equilibrium constant
is temperture dependent
592
larger Keq
other R the eqilibrium is
593
reverse reaction of equilibrium is
1/keq
594
Keq
= [products]/[reactants]
595
le chatliersqif stress i
s applied ot the sstem, the sstem shifts to relieve that applied stressed
596
at lower temp with a smaller heat transfer
a kinetic product forms
597
at higher temp with a larger heat transfer
thermodynamic prodict
598
density =
mass over volume (m/v) | kg/m^3 units
599
denisty of water
1 g/cm^3 = 1000 kg/m^3
600
Weight (Fg) =
density x volume x 9.8 (accelrtion due to gravity)
601
specific gravity
SG = density/1 g/cm^3/1 000 kg/m^3
602
pressure =
Force/Area | Pa= N/m^2
603
conversions between pressures
1.013 x 10^ 5 Pa = 760 mmHg = 760 torr= 1 atm
604
absolute hydrostatic pressure
total [ressure exerted on an object that is submerged in a fluid (liquids and gases) P= P0 + density(9.8)(z) z= depth P0= ambiant pressure, pressure on the surface, mopstly atm
605
guage pressure
difference between teh absolute pressure inside somewhere and the atmospheric pressure outside the place P gauge = P-Patm
606
density is directionless
therefore scalar
607
cohesion
attractrive force experienced by molecules ofr a fluid of the same
608
ahdesion
attractive forces experienced by molecules of a fluid for a sdifferent molecule
609
adhesive adn cohesive forces are equal
no meniscues form and liquid surface is flat
610
molarity
the number of moles of solute per liter of solution: 1 M = 1 mol/L
611
mol
item times avos number: 6.022 x 10^23
612
molarity times volume (in liters) equals
the number of moles of a substance that are present (mol = M × V).
613
millimolar (mM), micromolar (µM), and nanomolar (nM) concentrations
1 × 10-3 M, 1 × 10-6 M, and 1 × 10-9 M
614
adding salt to water causes BP of water to
increase, requiring a greater average kinetic energy of the liquid to produce a vapor pressure equal to the external pressure. lowering melting point
615
boiling water
pressure of the atmosphere = pressure to vaporize
616
Vapor pressure
the pressure of the vapor phase that exists (to some degree) immediately above the surface of any liquid. A higher vapor pressure indicates that a larger number of solvent particles were able to escape the liquid and enter the gas phase. When vapor pressure is equal to the atmospheric pressure exerted on the liquid’s surface, the liquid will boil. more solute particles causes a reduction in vapor pressure
617
BP = vapor pressure reduction
the lower the vapor pressure, the more energy that will be required to increase that vapor pressure to a level that matches the atmospheric pressure. In other words, the more solute particles present, the lower the vapor pressure, and the higher the boiling point.
618
freezing point depression
solute molecules disrupt the lattice structure of the frozen solvent, so more added solute corresponds to more “difficulty” freezing and a lower freezing point.
619
why solid ice is more dense than liquid
The bent structure of the water molecule and ratio of covalently-bonded hydrogens to lone pairs of electrons on the oxygen atom maximizes the hydrogen bonding that occurs in the solid phase, producing a hexagonal structure with large empty spaces. negative slope bc solid less dense than liquid
620
SO32-
sulfite
621
SO42-
sulfate
622
Ionic compounds
one or more cations (positively-charged ions) paired with one or more anions (negatively-charged ion no net overall charged
623
in β-minus decay, a neutron is converted to a proton as an electron is emitted.
define
624
Boiling chips
provide nucleation sites that give the liquid a place to start forming bubbles to prevent superheating
625
vacuum distillation
lower the boiling points of the substances to be distilled.
626
aldehydes have lwer boiling points than hydrogen bonding
aldehydes end in -al , hydrogen bonding/carb acid end in -oic acid
627
Formal charge =
of valence electrons - sticks - dots
628
N has
5 valence electrons
629
The preferred ion configuration of many elements
the electron configuration of the nearest noble gas; elements will gain or lose electrons until they have the same valence electron configuration as this noble gas. complete octet
630
The attractive force of this positively-charged nucleus on the atom’s negatively-charged valence electrons is termed the effective nuclear charge (Zeff). `
As the number of protons in the nucleus increases from left to right across a period (or row) of the table, Zeff also increases, since each additional proton adds positive charge to the nucleus.
631
the atoms with the largest radii
bottom left
632
ionic radius
cations (positive ions) tend to have smaller ionic radii than the atomic radii of their corresponding uncharged elements. This is because an uncharged atom must lose one or more electrons to become positively charged. On the other hand, for anions (negative ions), the ionic radius is typically larger than the corresponding atomic radius, since these species must gain electrons, and thus become slightly larger, to take on their negative forms.
633
torque
``` frsin theta perpendicular sin (90)= 1 ```
634
calculations
v = (6 mm) / (0.2 s) = 30 mm/s = 3 x 10-2 m/s
635
Competitive inhibitors increase the Km of their associated enzymatic reactions without altering the Vmax value,
fact
636
km
Km is the substrate concentration required to reach Vmax/2
637
Competitive inhibition is when the inhibitor directly competes with the substrate for the active site on the enzyme.
This increases Km since it now takes more substrate to ensure half of the active sites are occupied. If enough substrate is supplied, it will outcompete the inhibitor; therefore, Vmax does not change, although more substrate is needed to reach it.
638
noncompetitive inhibition,
Vmax is decreased. Since these inhibitors do not compete with the substrate, their activity is unaffected by substrate concentration. Since the inhibitor always affects a consistent proportion of the available enzyme, Vmax is reduced.
639
Uncompetitive inhibition
thereby decreasing Vmax. Km also decreases to exactly the same degree as Vmax.
640
N2
a very inert gas (Noble) and therefore unreactive
641
power
v^2/r
642
paraell
1/r + 1/r
643
terpenes
think hormones
644
IR peaks 1700-1750
C=O
645
Ir peaks 3200 3500
-OH
646
homotropic regulation
when a molecule serves as a substrate for its target enzyme, as well as a regulatory molecule of the enzyme's activity. O2 is a homotropic allosteric modulator of hemoglobin. The four subunits of hemoglobin actually bind to oxygen cooperatively, meaning the binding of oxygen to one of the four subunits will increase the likelihood that the remaining sites will bind with oxygen as well. This is the cause of the sigmoidal curve shown in the figure.
647
indicator in pH
usually near ht desired pH | weak acid and strong base- around 9! or greater than 7
648
THIOL
R-SH
649
amide
[R(C=O)NR]
650
amine
(R-NR2)
651
ester
R(C=O)OR’
652
sulfoxide
[R–S(=O)–R']
653
solid to liquid to gas
endothermic | absorbing heat
654
gas to liquid to solid
release heat, making them exothermic reactions
655
isomers
he same molecular formula) but different structural or spatial arrangements of these ingredients.
656
chain isomers
diff Skelton arrwangement
657
functional isomers
isomers where the molecular formula remains the same, but the type of functional group in the atom is changed. For example, a compound with an oxygen atom in addition to several carbon atoms and the corresponding number of hydrogens could be an alcohol with an –OH group, or an ether with a C–O–C group.
658
Positional isomers
given functional group in different locations (e.g., 1-pentanol vs. 2-pentanol).
659
Stereoisomers
involve different ways that substituents can be positioned. Cis (Z) -trans (E) isomerism
660
work
W = F⋅d⋅cos(θ) delta KEf - KeI which can equal PE ?
661
power=
work/time
662
Watt =
J/s
663
1 Kw
1000 J/s
664
(P = Fv)
constant force times constant velocoty
665
P = IV)
current and velocity
666
E = hc/λ,
``` h = Planck’s constant (6.62 x 10-34 J•s) C = speed of light = (3 x 108 m/s) E = given = ```
667
Cupric
"Cupric" tells us that we are using the Cu2+ (or copper [II]) cation.
668
highest Ka
A higher Ka is associated with stronger acidity. dding electron-withdrawing functional groups (like fluorine atoms) provides inductive stabilization of the conjugate base by pulling electron density away from the negatively-charged position (shown below). This stabilization increases the acidity of the original compound. Inductive effects increase if the electron-withdrawing groups are closer to the acid and if more of them are present.
669
oxidative phosphorylation
phosphorylate ADP into ATP is final step is the process in which ATP is formed as a result of the transfer of electrons from NADH or FADH 2 to O 2 by a series of electron carriers. This process, which takes place in mitochondria, is the major source of ATP in aerobic organisms
670
V = 2πr/T
yep
671
Fc = mv2/r
yes
672
suciice inhibitor
suicide inhibitor acts as an irreversible enzyme inhibitor. occurs when an enzyme binds the inhibitor (structurally a substrate analogue) and forms an irreversible complex with it, usually through a covalent bond. This can involve the inhibitor being chemically modified by the enzyme during the normal course of catalysis to produce a reactive group that is specifically responsible for the formation of the irreversible inhibitor-enzyme complex.
673
only amino acid that is chiral is
glycine (G)
674
thin layer chromatography with a silica plate
polar substance will move slower on the plate due to polar-polar interactions between the substance and the plate. This means that the Rf value of a polar substance will be smaller than that of a nonpolar substance since the substance will move less on the plate compared to the solvent front than a nonpolar substance would.
675
imine
C=N
676
benzenes are
Benzene, the aromatic hydrocarbon shown below, is very stable (inert) in the presence of acids and bases and will not react with the reagents.
677
speed =
max flow rate x area | example- -screenshot
678
Pyruvate dehydrogenase
is the enzyme that mediates pyruvate decarboxylation. This step is the critical link between anaerobic and aerobic respiration. With this link broken, cells would be limited to anaerobic respiration. Thus, a decrease in aerobic respiration makes sense in this context acetyl COA is product and NADH
679
geometric isomers
each of two or more compounds which differ from each other in the arrangement of groups with respect to a double bond, ring, or other rigid structure.
680
epimers
an epimer is one of a pair of diastereomers. The two epimers have opposite configuration at only one stereogenic center out of at least two. All other stereogenic centers in the molecules are the same in each.
681
anomers
An anomer is an epimer at the hemiacetal/hemiketal carbon in a cyclic saccharide, an atom called the anomeric carbon.
682
imide
n organic compound containing the group —CONHCO—, with double bonded Oxygens at end
683
urea
Nh2 on either side of the carboxylic acid
684
acetate
Ch3 to a carboxylic acid to a oxygen
685
ether
r-o-r
686
ester
r to carboxylic acid to oxygen to r
687
uv spec
measures conjugation | double bonds
688
conjugation
Conjugation refers to the presence of alternating double bonds within the structure of an organic molecule. From its name alone, we can see that 1,3,5,7-octatetraene has such a structure.
689
ammeter
measures current
690
Moving from a lower to a higher energy level is associated with absorption of energy,
emission is associated with moving from higher to lowe
691
The question stem states that free radicals can cause cancer, which is a result of poorly regulated cell growth and division. Cancer is generally a product of mutations in DNA that disrupt these processes. Therefore, we must choose the answer that targets DNA.
nucleic acids
692
gamma particle
has no mass
693
alpha partlce
has the most mass with 2 protons and 2 neutrons
694
SDS page
SDS-PAGE is an electrophoretic technique which involves the binding of the anionic detergent SDS to a polypeptide chain. SDS binding denatures and imparts an even distribution of charge per unit mass to the protein, resulting in fractionation by approximate size alone during electrophoresis.
695
D and L are
releative configurations
696
R and S
absolute configurations
697
weak acid
HF due to covalent bonding
698
galvanic cells
The passage states that the cell is meant to act like a galvanic cell, meaning that it proceeds in a spontaneous fashion. Since galvanic cells always have cell potentials that are greater than 0, we can eliminate any negative options
699
calcium carbonate
CaCO3
700
Phosphorous acid
H3PO3
701
Phosphoric acid
H3PO4
702
perphosphoric acid.
H3PO5
703
hypophosphorous acid.
H3PO2