Final Review Part I: Lectures 1-10 Flashcards

(90 cards)

1
Q

What is? Inductive Reasoning

A

Predictive generalizations that are based on a large number of observations. EX: We predict that the sun will rise in the east tomorrow morning based on past experiences of the sun doing just that.

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2
Q

What is? Induction Based Science

A

makes predictions based on past
experience; an example of induction-based science is the development of “Cell
Theory”, a series of generalizations about cells based on observing many cells

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3
Q

Hypothesis Based Science

A

uses deductive reasoning (maybe; there is some
controversy about this); hypothesis-based science gets most of the attention from
philosophers of science

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4
Q

Deductive Reasoning

A

reasoning from more general statements to a
conclusion that must be true; e.g. (from Wikipedia)
1) All men are mortal.
2) Socrates is a man.
3) Therefore, Socrates is mortal.

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5
Q

Hypothesis

A

tentative explanation for an observation

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6
Q

Hypothetico-Deductive Method

A

one possible description of the method of
hypothesis-based science; hypotheses are tested by the use of experiments; the
outcome of the experiments is predictable based on the hypotheses; if the
outcomes of the experiments are inconsistent with the predictions, then the
hypothesis is rejected (it is wrong/incorrect/refuted/rejected); alternatively, if the
outcome of the experiments are consistent with the predictions for the outcomes,
then we have support for the hypothesis (but support ≠ “proof”)

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7
Q

Testable Hypothesis

A

a hypothesis which can provide testable predictions for

outcomes of experiments

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8
Q

Non-Testable Hypothesis -

A

a hypothesis which cannot provide testable predictions;
such a hypothesis is not necessarily incorrect, the scientific method simply can’t
deal with it

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9
Q

Occam’s (Ockham’s) Razor

A

– If several explanations are compatible with the evidence
at hand, the simplest should be considered the most likely; alternative version:
explanations should be no more complicated than necessary; named after William
of Occam (who was not the inventor of the idea, but who popularized it)

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10
Q

Importance of the “Control”

A

all scientific experiments must have “controls”, which
act as comparisons for “treatments”; without controls it is impossible to know
whether the treatments have had an effect (e.g. would the observed outcome have
occurred even in the absence of the treatment?)

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11
Q

Negative and Positive Controls

A

this difference was not discussed in lecture (i.e. this is
for interest only); negative controls are experiments in which nothing is done or
added (there is no “treatment”); positive controls are controls in which a certain
treatment has a known effect, and this known effect is used to compare with
treatments of unknown effect; almost all experiments have negative controls;
depending on the type of experiment, there may or may not be positive controls
incorporated into the overall design of the experiment

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12
Q

Composition of an Atom

A

nucleus composed of protons (+1 charge) and neutrons (no
charge); electrons (-1 charge) in orbitals around the atom; electrons are much
smaller than protons or neutrons; there are many ways of indicating orbitals in
diagrams; we will diagram orbitals simply as circles around the nucleus

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13
Q

The Number of Protons Defines the Type of Atom

A

e.g. hydrogen (H )atoms have one
proton, helium (He) atoms have two protons, carbon (C) atoms have 6 protons,
oxygen atoms (O) have 8 protons

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14
Q

Bonds between Atoms are Based on Electrons

A

there are possibly single, double or
triple bonds between two atoms; quadruple bonds do not exist; a chemical bond is
based on a pair of electrons, one electron provided by each atom

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15
Q

Hydrogen (H)

A

smallest atom, composed of one electron and one proton; if a H atom
loses an electron, only the proton remains – this is shown as H+
(i.e. “H+” and
“proton” are synonymous; protons are very important in later discussions of
respiration and photosynthesis).

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16
Q

Ions

A

atoms or molecules in which the number of protons ≠ the number of electrons

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17
Q

Cations

A

positively charged ions, in which there are more protons than electrons

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18
Q

Anions

A

negatively charged ions in which there are fewer protons than electrons

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19
Q

Hydrogen Bonds (H bonds)

A

are weak, transient (constantly breaking and re-forming)
bonds, and are a consequence of polar covalent bonds containing H. Liquid water is
the classic example used to illustrate H bonding. Water is a small molecule, and almost
all other molecules of similar size are gases at room temperature. Water is a liquid at
room temperature because of H bonding: the δ+ of the H atoms (δ+ because they are
in polar covalent bonds with O) on water molecule are attracted to the δ- on the O
atoms of other water molecules. Although H bonds are weak and transient, at any
instant in time there are a lot of them. See diagram next page.

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20
Q

Electronegativity

A

the ability of an atom to attract electrons to itself; a fixed property
of atoms

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21
Q

Non-Polar Covalent Bond

A

a chemical bond between two atoms in which electrons in
the bond are shared equally between the atoms; occurs when there are bonds
between like atoms, e.g. O=O, H-H, or between atoms that have very similar
electronegativity e.g. C-H bonds; there are no partial charges associated with
these bonds

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22
Q

Polar Covalent Bond

A

a chemical bond between atoms of moderately different
electronegativity; results in unequal sharing of electrons in the bond, with the
electron air displaced towards the atom with higher electronegativity; results in
partial charges (δ+, δ-
); important polar covalent bonds in biology include: O-H,
N-H, O-C, N-C

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23
Q

Ionic Bond

A

a chemical bond between atoms of greatly differing electronegativity;
electrons in the bond are not shared, but rather the atom with higher
electronegativity takes an electron from the atom with lower electronegativity

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24
Q

Polar Molecules

A

have many polar covalent bonds, and thus have partial charges;
there are degrees of polarity, with the number of polar covalent bonds compared
to other types of bonds determining the degree of polarity; small polar molecules
tend to be highly water soluble

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25
Polar Covalent Bonds Containing H
will lead to the possibility for H-bonding – water is | a standard example of H-bonding, with the δ+ of the H atoms is attracted to the δof O atoms on nearby water molecules
26
Hydrogen (H) Bonds
weak transient bonds caused by polar covalent bonds | containing H
27
Water Molecule
polar covalent bonds containing H lead to partial charges, and thus to the possibility for H-bonding; the extensive H-bonding in water causes it to be a liquid at room temperature; other molecules of similar (low) molecular mass all are gases at room temperature (note that molecules other than water can exhibit Hbonding as well; H-bonding is not restricted to water)
28
Water Exhibits Cohesion
due to H-bonding, water molecules are attracted to each other; they stick to each other; this explains the liquid nature of water at room temperature; also explains surface tension
29
Water Exhibits Adhesion
water is attracted to large polar/charged molecules; water is attracted to those molecules, even though the molecules are too large to be dissolved; explains the “meniscus curve” of a graduated cylinder or other glassware
30
Hydrophilic
literally means “water-liking”; hydrophilic molecules are polar and/or charged, and exhibit mutual attraction with water molecules
31
Hydrophobic
literally means “water-fearing”; hydrophobic molecules are composed largely of non-polar covalent bonds (e.g. as fats); hydrophobic molecules exhibit mutual repulsion with water
32
Dissociation of Water
H2O H+ + OHThe dissociation can also be thought of as: 2 H2O H3O+ + OH- (H3O+ = the hydronium ion) Acidity – think of acidity as H+s (protons); high acidity = high [H+] pH – measure of acidity; pH = -log[H+]; pH 7 is considered to be “neutral”, pH < 7 is “acidic”, and pH > 7 is “basic” pH of pure water (no dissolved gases) = 7 pH of lemon juice ~2 pH of household bleach ~12 Hydrochloric Acid – a strong acid; shows complete dissociation, unlike the equilibrium for the dissociation of water: HCl H+ + ClEffect of atmospheric CO2 on the pH of water – CO2 reacts with water to produce carbonic acid, which causes the water to acidify (increase in [H+]): CO2 + H2O H2CO3 H+ + HCO3 - carbonic bicarbonate ion acid
33
Water PH
The pH scale measures the concentration of hydrogen ions (H+) in a solution. (credit: modification of work by Edward Stevens). From OpenStax Biology. Note: the pH of distilled water (= pure water) is 7 only if it is completely pure water. Contact with air, which contains CO2, will cause the water to acidify due to carbonic acid formation.
34
Water Hydrogen Bonding
Cyclic dimer of acetic acid; dashed green lines represent hydrogen bonds. That is, H bonds don’t occur only in water. H bonds are very common, and crop up numerous times in biology, e.g. in the structure of the DNA double helix.
35
Water as a Solvent
the polar covalent bonds of water, which lead to a δ- on the O and a δ+ on the H, cause water to be a polar molecule; as such, water is a good solvent for small polar and charged molecules (which are hydrophilic)
36
Effect of Molecule Size on Water Solubility
the solubility of polar molecules decreases as the molecules get larger; the reasons for the decrease in solubility with larger size are complex and only partially understood
37
Molecules with Mainly C-H and C-C Bonds are not Water Soluble
these molecules do not have partial or full charges, and do not interact with water, i.e. they are hydrophobic and are not water soluble; a common example is vegetable oil, which does not mix with water; water is not a universal solvent
38
Life is Carbon-Based
if you remove the water from an organism, what’s left is mainly carbon; all biological molecules are C-based (although different types of atoms are may be attached to the C-based molecules); the key to understanding the C basis of life is that C is extremely versatile; think of it as a Lego block
39
Carbon atoms always have four bonds
could be four single bonds, two singles and a | double, two double bonds, or a single and a triple bond
40
Carbon Electronegativity
C has a moderate to low electronegativity
41
Non-Polar Covalent Bonds
C-C and C-H bonds are non-polar covalent; C and H have | virtually the same electronegativity
42
Polar Covalent Bonds
C-O, C-N bonds are polar covalent; O and N have higher | electronegativity than C, therefore C will have a δ+ charge while O or N will have a δcharge
43
Carbon-Based Molecules May Exhibit Isomerism
there are three main types of isomerism, listed below (molecules that are isomers have the same molecular formula but different structures)
44
Structural Isomerism
when different molecules have the same molecular formula | but differ in how C atoms are arranged, e.g. C4H10 may be assembled in two ways
45
Cis/Trans Isomerism (part of Geometric Isomerism)
when different molecules have the same molecular formula, but differ in how parts of the molecule are assembled around a C=C bond; based on the fact that C=C bonds are inflexible and do not allow rotation
46
Enantiomers
occur when a C atom has 4 different things attached; this C atom is termed as being “asymmetric” or “chiral”; molecules that are enantiomers have the same molecular formula but are mirror images of each other; a common analogy is that the left and right hands of humans are mirror images of each other
47
Bonds with Carbon can be arranged in three dimensions
if there are four single bonds, the bonds are definitely in three dimensions. Consider methane (largest single component of natural gas), which has the molecular formula CH4. Methane is often drawn as a flat molecule:
48
Structural Isomers
have the same molecular formula but differ in the arrangement of the C atoms. Both molecules shown below have the formula C4H10 (images from Wikipedia).
49
Cis/Trans Isomers (which are a subset of Geometric Isomers)
occur when there is variation in arrangement around a C=C bond. But for cis/trans isomers, both of the isomers have exactly the same atoms joined up in exactly the same order. C=C bonds cannot rotate, thus the two molecules shown below are different molecules with slightly different chemical properties (images from Wikipedia).
50
Enantiomers
occur when there are C atoms with 4 different things attached. These C atoms are called “chiral” or “asymmetrical”. In the example below, the central (chiral/asymmterical) carbon has 4 different things attached to it, and there are two ways to do the attachment. This leads to different molecules that are nonsuperimposable mirror images of each other. Two forms of lactic acid are shown below (image from Wikipedia).
51
Isomerism of Carbon-Based | Molecules
``` Molecules that have the same number and type of atoms arranged differently are called isomers. (a) Structural isomers have a different covalent arrangement of atoms. (b) Geometric isomers have a different arrangement of atoms around a double bond. (c) Enantiomers are mirror images of each other. ```
52
Macromolecules
very large biological molecules; polymers composed of many monomer subunits; synthesized by condensation synthesis (= dehydration synthesis); carbohydrates, proteins and nucleic acids are macromolecules
53
Large Biological Molecules
biological molecules not quite as big as macromolecules, | e.g. lipids are considered to large biological molecules rather than macromolecules
54
Monomer
``` building block (subunit) of a polymer, e.g. monosaccharides are the monomers that are linked together to produce polysaccharides (a polymer) ```
55
Polymer
a large molecule composed of numerous linked monomers; the monomers are linked by covalent bonds
56
Condensation Reaction/Dehydration Reaction –
formation of a covalent bond with the | loss of a water molecule
57
Condensation Synthesis/Dehydration Synthesis
several to many rounds of condensation reactions, leading to the formation of large biological molecules or macromolecules
58
Hydrolysis
break apart with water; opposite of a condensation reaction
59
Hydrolysis of Macromolecules
Why do it? – to remove damaged macromolecules or macromolecules that are no longer needed; the monomer subunits of the macromolecules can be recycled to produce new macromolecules
60
Carbohydrates
sugars or sugar-derived molecules; include monosaccharides (which are monomers), oligosaccharides (2+ linked sugar monomers, but smaller than a polysaccharide), and polysaccharides (100s to 1000s of linked sugar monomers); carbohydrates contain many polar covalent bonds (O-H, O-C) and are thus hydrophilic; smaller carbohydrates are easily water soluble
61
Starch Versus Cellulose
both are glucose polymers; starch is held together by α-1,4 bonds, which the human digestive can break apart and thus access the glucose as an energy source; cellulose is held together by β-1,4 bonds which the human digestive system cannot break apart, hence cellulose (which is a major component of plant cells) is not an energy source for humans
62
Lipids
large biological molecules that mix poorly with water, if at all; fats (which include oils), phospholipids, steroids; fats and steroids are hydrophobic and do not mix with water at all
63
Fats (= Triglycerides)
three fatty acids attached to glycerol (3C molecule); extremely hydrophobic; used as energy storage molecule
64
Saturated Fat
has only C-C bonds in the fatty acids
65
Unsaturated Fat
has a C=C bond in the fatty acids
66
Polyunsaturated Fat
has 2+ C=C bonds in the fatty acids; but the majority of the | bonds are C-C
67
Oil
a fat that is liquid at room temperature (due to C=C bonds in the fatty acids, which introduce kinks/bends and thereby prevent close packing of the molecules)
68
Phospholipids
composed of glycerol (3C molecule) + 2 fatty acids and a head group; the head group contains phosphate (PO4 3- ) plus an “R” group; the R group is either charged or polar; because of this structure, phospholipids are partly hydrophobic (the fatty acids) and partly hydrophilic (the head group) – thus phospholipids are amphipathic molecules (part of the molecule is hydrophobic and part of the molecule is hydrophilic)
69
Phospholipid Bilayers
form the basis for biological membranes; they have a hydrophobic core, and water molecules are associated with the hydrophilic head groups
70
Steroids
non-fatty acid-based lipids; have 4 carbon-based rings; are hydrophobic; there are many types of steroids, but all have similar structures; are components of membranes, and are also hormones (e.g. progesterone, testosterone)
71
Proteins
polymers of amino acid monomers; have various levels of structure
72
Amino Acids
most amino acids have the same basic structure; the individual amino acids are defined by their “side chains” or “R groups”
73
Protein Amino Acids
there are 20 protein amino acids; plants can synthesize all 20 of these amino acids; animals cannot synthesize all of the amino acids; for animals, amino acids that cannot be synthesized must be provided in the diet – these are known as “essential amino acids”
74
Nucleic Acids
polymers of nucleotide monomers; DNA and RNA; DNA is composed of DNA nucleotides (containing the 5C sugar deoxyribose), RNA is composed of RNA nucleotides (containing the 5C sugar ribose)
75
Nucleotide
nucleic acid monomer; contains a 5C sugar, a nitrogenous base and a phosphate group
76
Nucleotide Nitrogenous Base
defines the type of nucleotide; both DNA and RNA are composed of 4 types of nucleotides; DNA is composed of A, T, C, G; RNA is composed of A, U, C, G
77
DNA is present as a double-stranded helix
the “double strand” is due to complementary pairing of nitrogenous bases; A has double H-bonds with T (A=T), and G has triple H-bonds with C (G≡C)
78
DNA Represents Information
genes” are mostly sequences of DNA nucleotides that | define the primary structure of proteins
79
Genetic information flow involves three types of macromolecules:
DNA RNA Protein transcription translation The above diagram shows the flow of information, not the flow of matter. In other words, the information represented by DNA is transcribed into the information represented by RNA, and the information represented by RNA is used to determine the primary structure (amino acid sequence) of a protein. Keep in mind that the information of DNA is in the form of a linear sequence of DNA nucleotides, that RNA’s information is in the form of a linear sequence of RNA nucleotides, and in the end, what we have is a sequence of amino acids (a protein). So, we are talking about three different types of macromolecule, all of which are composed of different types of monomer subunits. Polymers and Monomer subunits Associated with Genetic Information Flow: DNA (= a macromolecule/polymer) subunits are DNA nucleotides (monomer) RNA (= a macromolecule/polymer) subunits are RNA nucleotides (monomer) Protein (= a macromolecule/polymer) subunits are amino acids (monomer)
80
Hydrolysis
• Macromolecules and large biological molecules are polymers composed of monomer subunits. • Condensation reactions (= dehydration reactions) link monomer subunits together. • A condensation reaction involves the removal of a water molecule from the two monomers, resulting in a covalent bond. • In a macromolecule, there are many monomer subunits linked together, and every monomer was added via an individual condensation reaction. Thus, there are many condensation reactions needed in order to produce a macromolecule. This process of repeated condensation reactions is known as condensation synthesis (= dehydration synthesis). • Macromolecules can also be broken down, via the process of hydrolysis. • Hydrolysis, in a simple sense, is the opposite of condensation synthesis. Hydrolysis literally means to “break apart with water”, and involves the re-addition of water molecule to break a covalent bond. • Both condensation synthesis and hydrolysis are tightly regulated by cells, and are catalyzed by enzymes (enzymes are discussed later in the course). • Macromolecules may be hydrolyzed because: 1) they are damaged, or 2) they are no longer needed. The monomer subunits resulting from hydrolysis can be recycled to produce other macromolecules
81
Carbohydrates
* simple sugars or polymers of sugar units | * probably the single most abundant group of biological molecules
82
Monosaccharides
simply a sugar monomer, e.g. glucose or fructose • C-based; the most common ones have 5 or 6 C atoms as a "backbone“; may contain from 3 - 7 C atoms • names typically end in “-ose” (also true for many oligosaccharides and polysaccharides) • highly H2O soluble (are small polar molecules) • most have a sweet taste • contain 2 or more -OH groups
83
Oligosaccharides
short chain of 2 or more sugar monomers • chain is formed by condensation synthesis between monosaccharide monomers • "disaccharides" are oligosaccharides composed of only 2 subunits; e.g. sucrose (table sugar) is composed of glucose-fructose • also includes trisaccharides and longer chains, up to perhaps 16 to 18 carbon atoms • the shorter chain oligosaccharides are highly water soluble, whole the longer chain oligosaccharides are less soluble and are typically found attached to proteins or lipids
84
Glucose
is a 6 carbon sugar, a monosaccharide, and an important source of energy in cells; in mammals it is “blood sugar”. Glucose is a small polar molecule and is highly water-soluble (due to the combination of partial charges and the relatively small size of the molecule). The partial charges of the molecule are due to the many O-H and O-C bonds (which are polar covalent bonds). Glucose is also the monomer subunit of polysaccharides such as starch and cellulose. In starch and cellulose the carbon #1 of one glucose molecule is attached to the carbon #4 of the adjacent glucose molecule via a condensation (dehydration) reaction.
85
Polysaccharides
the true macromolecules among the carbohydrates • extremely long chains of sugar monomers; typically 1000's of linked monomers • form as a result of many condensation reactions • generally only poorly water soluble, but do attract water (they are hydrophilic); are hydrophilic because of the many polar covalent bonds • polysaccharides that are glucose polymers are starch, glycogen and cellulose; starch is an important plant C storage compound, and glycogen serves that function in animals; cellulose is an important component of plant cell walls • starch/glycogen have α-1, 4 linkages between the C atoms of adjacent glucose units; these are easily hydrolyzed by mammals (including humans); hydrolytic breakdown of starch/glycogen yields glucose (= an energy source); the hydrolysis is done by specific enzymes • cellulose has β-1,4 linkages ; not easily hydrolyzed by mammals; mammals such as cattle have microbes in their digestive systems that are able to hydrolyze β-1,4 linkages; humans are not able to hydrolyze β-1,4 linkages, therefore cellulose is not an energy source for humans (acts only as a component of “dietary fibre”)
86
Lipids
• Are often classified as large biological molecules rather than macromolecules. • Three sub-types of lipids: fats, phospholipids and steroids; fats and steroids are hydrophobic, while phospholipids are amphipathic.
87
Fats
are composed of a three carbon (3C) backbone (glycerol) with three fatty acids attached (via condensation/dehydration synthesis).
88
Fats versus Oils
oils are simply fats that are liquids at room temperature; same basic structure of glycerol + 3 fatty acids; difference is that fats have saturated fatty acids while oils have unsaturated or polyunsaturated fatty acids; the kinks/bends introduced by the C=C bonds hinders close packing of the oil molecules, and they remain liquid at room temperature (they will solidify if the temperature is lowered sufficiently); fats, with saturated fatty acids, exhibit close packing at room temperature
89
Phospholipids
similar, but not identical structure to fats; composed of glycerol plus two (not three) fatty acids; the third fatty acid is replaced by a hydrophilic head group • the head group contains phosphate (which is charged); the phosphate is attached to the glycerol; as well, there is another group (the “R group”) that is attached to the phosphate; the R group varies among different phospholipids, but is always either polar or charged • thus phospholipids have a hydrophobic portion of the molecule (the fatty acids) and a hydrophilic portion (the head group); molecules that are partly hydrophobic and partly hydrophilic are called amphipathic • in contrast to fats, phospholipids play a structural role in cells; biological membranes are composed of a phospholipid bilayer with associated proteins
90
Steroids
• hydrophobic, non-fatty acid-based lipids • there are many types of steroids, but all have the same basic structure (four Cbased rings); different steroids have different atoms attached to various parts of the basic steroid structure • play two major roles: hormones (there are many steroid-based hormones, e.g. estrogen and testosterone) and structural (steroids are components of biological membrane, and influence the “fluidity” of the membranes)