Chapter 11 Flashcards

1
Q

What is the temperature gradient in fractional distillation

A

Hot at the bottom colder at the top

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Steps of fractional distillation

A

Crude oil heated to above 350 and vaporised and put into column
When the top drops below a hydrocarbons boiling point it condenses
Fractions made with hydrocarbons with similar mp and bp

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How does the viscosity bp and flammability change going up the column

A

Bp decreases
High viscosity———> low viscosity
Flammability increases ( short chain hydrocarbons ignite more easily)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How many bonds can carbon form

A

4

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Define hydrocarbon

A

Organic compounds that contain carbon and hydrogen only

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is a saturated hydrocarbon

A

Single bonds only

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is an unsaturated hydrocarbon

A

Carbon -carbon multiple bonds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Functional group

A

Part of the organic molecule responsible for its chemical reactions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Homologous series

A

Series of organic compounds with the same functional group but with each successive member differing by CH2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

General formula for alkanes

A

CnH2n+2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is aliphatic

A

Hydrocarbons with carbon atoms joint in straight or branches chains

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is Alicyclic

A

Hydrocarbon with carbons atoms joined in a ring structure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is aromatic

A

Some or all carbon atoms found in a benzene ring

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the homologous series of aliphatic hydrocarbons

A

Alkanes
Alkenes
Alkynes ( triple bond)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How do you name branches

A

Use stem for the number of carbons and add yl
Eg methyl
Ethyl
Propyl

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How do you name a hydrocarbon with more then one alkyl group on the main chain

A

Alphabetically

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

General formula for cycloalkanes

A

CnH2n

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Alcohol
Functional group
Prefix
Suffix

A

OH
Hydroxyl
Ol

19
Q

Haloalkane
Functional group
Prefix

A

F, Cl,Br,I
Fluoro, chloro, bromo, iodo

20
Q

Aldehyde
Functional group
Suffix

A

H /C=O carbon double bonded to oxygen diagonally right up amd single bonded to h diagonally right down
Al

21
Q

Keytone
Functional group
Suffix

A

C-c=O-c double bond to O in the middle and vertically up
One

22
Q

Carboxylic acid
Functional group
Suffix

A

COOH double bind for O single bond for OH
Oic acid

23
Q

What is an empirical formula

A

Simplest whole number ratio of atoms of each element

24
Q

Molecular formula

A

The actual number of atoms of each element in a molecule

25
General formula
Simplest algebraic formula for a member of a homologous series
26
General formula for alkenes
CnH2n
27
General formula for alcohol
CnH2n+1OH
28
Displayed formula
Drawn out
29
Structural formula
Shorthand form of displayed formula Eg Ch3CH2Ch2CH3
30
Skeletal formula
Each end of line is a carbon Use parallel lines for double bonds
31
Define structural isomers
Molecules with the same molecular formula but with different structural formulas
32
Chain isomerism
Carbon chain is different
33
Position isomerism
Functional group in a different position on main hydrocarbon chain
34
Functional group isomerism
Functional group is different
35
How do you represent a branch in a structural formula
Put it in brackets
36
How can a covalent bond be broken
In two ways Homolytic fission Heterolytic fission
37
Homolytic fission
Each bonded atom takes one of the shared pair of electrons Each atom has an unpaired electron- a free radical Two species of the same type are produced X-Y ——> X. +Y.
38
Hetrolytic fission
One of the bonded atoms takes both the shared pair of electrons Two ions produced One negative (anion) and one positive (cation) X-Y——>X+ + Y-
39
Heterolytic fission with curly arrows
The species taking the electrons has an arrow from the middle of the bond to that species
40
Homolytic with curly arrows
2 half headed arrows from the middle of the bond to both elements
41
Addition reaction
100% atom economy Two reactants combined to make one product One molecule added across the double bond
42
Substitution reaction
An atom or group of atoms is replaced with a different atom or group of atoms
43
Elimination reaction
One reactant reacts to form 2 products A molecule is removed from a saturated molecule to make a unsaturated molecule