Organic Chemistry Flashcards

1
Q

Is alkanes saturated or unsaturated?

A

Saturated

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

Which hydrocarbon undergoes complete combustion?

A

Alkane

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

Which hydrocarbon undergoes incomplete combustion?

A

Alkene

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

Functional group of carboxylic acids

A

COOH

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

Displayed formula of carboxylic acid

A

C = O
|
O-H

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

Functional group of alkene

A

C=C

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

Functional group of alcohol

A

OH

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

Formula for alkane

A

CnH2n+2

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

Formula for alcohols

A

CnH2n+1OH

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

What is a diol?

A

An alcohol group with OH at both ends

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

Sequence of alkenes

A

EPBPe

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

Sequence of alcohols

A

MEPBPe

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

Sequence of carboxylic acids

A

MEPB

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

Sequence of alkanes

A

MEPB

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

Formula for carboxylic acid

A

CnH2n+1COOH
N MEANS CARBON -1 BECAUSE OF FUNCTIONAL GROUP

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

What hydrocarbon forms addition polymers

A

Alkenes eg poly(propene)

17
Q

What 2 monomers form a condensation polymer?

A

Diol and dicarboxylic acid group

18
Q

How do you produce esters?

A

React alcohol with carboxylic acid

19
Q

Esters uses

A

Perfumes, food flavouring and adhesives

20
Q

Carboxylic acid salts ending

A

-anoate (magnesium ethanoate).

21
Q

Potassium dichromate colour change

A

Orange to green

22
Q

Conditions for hydrogenation

A

Alkene to alkane
60°c with nickel catalyst

23
Q

Conditions for esterification

A

Carboxylic acid and alcohol with sulphuric acid catalyst

24
Q

Ester functional group

25
Conditions for alkene to alcohol
Alkene + steam -> alcohol 300°c with 60-70Pa and a phosphoric acid catalyst
26
Product naming of alkene + halogen reaction
Di + bromo/chloro/iodo + alkene but ane ending
27
What are the two ways of making alcohols
Steam + alkene or fermentation
28
Conditions for fermentation for alcohols
37°c and NO OXYGEN
29
Equation for fermentation for alcohols
Sugar (react with yeast) = ethanol + CO2
30
Properties of alcohols
Flammable, soluble in water and poisonois
31
Properties of hydrocarbons
Shorter chain = less viscous, lower melting point (more volatile) and more flammable
32
Positives and negatives of fermentation over hydration of ethene to make alcohols
Renewable, less energy BUT Slower, batch process and impure product
33
Negatives of hydration of ethene to make alcohols
Ethene from crude oil, not renewable, more energy
34
Positives of hydration of ethene to make alcohols
Faster, continuous process and pure product
35
Examples of natural polymers
Cellulose, DNA, proteins and starch
36
What does diol monomers lose in condensation polymerisation?
H molecules at both ends
37
What does dicarboxylic acid monomers lose in condensation polymerisation
OH molecules at both ends
38
What is an amino acid polymer called?
Polypeptide
39
What is a polypeptide made of
amino acid group and carboxylic acid group