Organic CHEM Flashcards

(41 cards)

1
Q

The physical properties of Alkanes

A

Properties that can be observed or measured without changing the composition of the substance

their solubility in water
their boiling point

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2
Q

Th boiling points of straight chain alkanes

A

Increases as the chain length increases

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3
Q

Boiling points of Alkanes

A

Boiling involves converting a liquid to a gas and requires energy (heat) to overcome the intermolecular interactions between molecules (Van-der Waals) attractions between molecules of alkanes

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4
Q

Non-Covalent intercations

A

do not involve sharing of valence electrons
these interactions are due to electrostatic interactions (attraction between opposite charges)
there are 2 categories: attraction between permanent and attraction between temporary partial charges

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5
Q

Attraction between permanent charges

A

Hydrogen bonds, salt ridges/ionic bonds, dipole-dipole interactions, ion-dipole interactions and dative bonds

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6
Q

Attraction between temporary partial charges

A

London dispersion forces (Van der Waals)

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7
Q

Hydrogen bonding

A

IUPAC definition:
hydrogen bonding occurs when an electron deficient hydrogen that is bonded to an atom, has an attractive interaction with another electron rich region either within the same or another molecular entity

for our purposes:
A hydrogen bond is the interaction of a hydrogen atom bonded to highly electronegative atoms (N,O,F) and the non-bonding electron pairs on other highly electronegative atoms

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8
Q

Salt bridges/ionic bonding

A

the name given by biochemists to the ionic bonds that form between the positively and negatively charged groups of amino acid side chains found in proteins

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9
Q

Dipole-dipole interactions

A

A polar covalent bond can also be called a permanent Dipole

when two permanent dipoles are in close proximity (such as carbonyl) , they will align themselves. The partially positive end of one dipole is attracted to the partially negative end of another.

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10
Q

Van der Waals forces (London dispersion forces)

A

Due to attractive interactions between temporary dipoles

all molecules experience these in addition to other types of interactions

they are the weakest type of intermolecular interaction and the only act over short distances

At any instant, electron movement in a molecule can create a temporary dipole with partial positive and negative charges

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11
Q

The temporary dipole of the first molecule

A

indices a temporary dipole in a molecule close by

there is a weak attractive force between oppositely charged parts of the molecule. Although the attractive interaction is very weak, in bulk media there can be lots of them so they are still important attractive forces

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11
Q

Important points to remember about van Der Waals forces

A
  1. They are bright about by a temporary dipole that induces another temporary dipole in a nearby molecule
  2. The are weaker than all other non-covalent attractive forces discussed and so relatively little energy is required to overcome them
  3. They act over very short distances compared to the other interactions we have discussed

short range - therefore they are more effective when the molecules are able to get closer together

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12
Q

Why the boiling point increases as the chain length increases

A

-The electrons in an alkane molecule are always moving
-When they become unevenly distributed over the surface of the molecule some regions of the surface have a slightly positive and others a slightly negative charge
-we say that the molecule is temporarily polarised
-the temporary polarisation of an alkane molecule induces the temporary polarisation in nearby alkane molecules
-then these molecules become weakly attracted to each other

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13
Q

Van der waals

A

operate over short distances and between the surfaces of the molecules, so molecules need to be close together to be attracted to one another

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14
Q

For straight chain alkanes

A

the larger the molecule (the greater the molecular weight of the alkane or the more carbon atoms in the chain) the higher the boiling point (as van der waal forces increase)

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15
Q

BUT for branched alkanes

A

The boiling points of alkanes with the same molecular weight decreases as you increase the number of branches.

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16
Q

In straight chain pentane

A

the surface area between the molecules is larger (molecules can get very close to each other) and so Va der waals attractions between them are greater than for spherical 2,2-dimethylpropane. Therefore, pentane has a higher boiling point

17
Q

Chemical changes causes

A

a change in the bonds of/between molecules, atoms or ions

18
Q

Physical changes causes

A

no change in bonding

19
Q

A new substance or substances is/are formed by

A

a chemical reaction

20
Q

The chemical reactions of alkanes

A

C-C bonds and C-H bonds are single (saturated hydrocarbons)
non-polar covalent
therefore, alkanes are relatively inert (unreactive)
they do undergo two main types of chemical reactions

21
Q

Combustion

A

A highly exothermic reaction (heat given out)
basis for use of hydrocarbons to provide heat and power
combustion of hydrocarbons produces CO2 (greenhouse gases)
incomplete combustion occurs if not enough oxygen present in this case carbon monoxide and carbon (soot) are formed as products of the reaction

22
Q

inert

23
Q

Halogenation

A

-A source of light or heat are required for the reaction to proceed
-example (The chlorination of methane)

24
The chlorination of methane
The reaction is a substitution reaction because a hydrogen atom of methane is substituted (replaced by) a chlorine atom in the product (chloromethane)
25
Carbon monoxide
binds to haemoglobin in blood as its the same shape as oxygen oxygen and carbon dioxide cannot be carried this is how people die from carbon monoxide poisoning
26
Substitution reaction (definition)
a reaction in which an atom or group is replaced (substituted) by another atom or group
27
What is the mechanism of reaction of the chlorination of methane
To break a covalent bond, the shared pair of electrons must leave that bond and they can do this in one of two ways 1: homolytic fission 2: heterolytic fission
28
Definition of mechanism of reaction
Detailed step by step changes that tale place during. reaction
29
Homolytic fission
The electrons in the bond are shared evenly between the two atoms; the bond is broken so that one electron remains with each of the 2 atoms The products of homolytic fission are free radicals The single, unpaired electron that came from the covalent bond is represented by a dot
30
A free radical
is an uncharged species with an unpaired electron free radicals are unstable; low stability => high energy they are reactive Eg. Cl(dot) is a chlorine radical
31
Heterolytic fission
The electrons in the bond are shared unevenly between the two atoms, one of the atoms from the bond takes both electrons white the there loses both electrons The products obtained will be a cation and an anion
32
Halogenation of alkanes occurs by
a chain reaction involving homolytic fission of bonds
33
Definition of a chain reaction
It requires energy in order to start, but once underway it will keep on going without requiring more energy input until all the reactants have been used up
34
The chlorination of methane, chain reaction involves 3 main steps
1. Initiation (generates radicals) 2. Propagation (radical at the start and radical at the end) 3. Termination (2 radicals at the start and none at the end)
35
Termination
If any two radicals combine, the chain reaction is terminated. There are three possible termination steps
36
Reaction scheme vs reaction mechanism
Reaction scheme: A + B -> C + D Reaction mechanism: Step 1: A reacts with B Step 2: A and B undergo___ Step 3: A + B reaction form C + D
38
39
The chlorine radicals produced when CFCs reach the stratosphere
Are ozone-removing agents and lead to destruction of the ozone layer
40
CFCs
Chlorofluorocarbons
41