Preview Cambridge Pre-U Chemistry Coursebook

Page 41

Syllabus content

Present?

Location

Coursebook

(C)oursebook or (S)upplement or (B)oth

Chapter number

Chapter title

Supplement

Section number

• addition polymerisation • elimination reactions

students should be able to: A3.5a

(a) compare C=C and C=O π bonds in terms of dipole moments to explain why there is no nucleophilic attack on C=C

Y

B

18

Carbonyl compounds

A3.5b

(b) describe addition reactions to C=C: the reaction with H3O +, HBr, H2 and Br2

Y

B

15

Hydrocarbons

A3.5c

(c) describe addition polymerisation as an example of an addition reaction and in terms of the repeat unit in the polymer; suggest the monomer given the structure of an addition polymer

Y

C

15

A3.5d

(d) understand that elimination reactions are essentially the reverse of addition reactions and that elimination competes with substitution, the former being favoured by high temperature and high pH

Y

B

16

A3.5e

(e) describe the formation of alkenes by the elimination of HX from alkyl halides or H2O from alcohols.

Y

C

16

A3.5e

(e) describe the formation of alkenes by the elimination of HX from alkyl halides or H2O from alcohols.

Y

C

17

A3.6

A3.6  Green chemistry

Start page

End page

To add to which chapter of Coursebook?

Section number

Title

• atom economy • reducing environmental impact

238

S18

S18.5

Nucleophilic addition to C=C

Addition reactions of the alkenes

208

209

S15

S15.5

Addition of aqueous acid, H3O +(aq)

Hydrocarbons

Addition polymerisation; Tackling questions on addition polymers

211

213

Halogenoalkanes

Elimination reactions

222

222

S16

S16.1

Elimination reactions

Halogenoalkanes

Elimination reactions

222

222

Alcohols, esters and carboxylic acids

5 Dehydration

230

230

W

238

R

Note that the application of green chemistry principles in question papers may not be restricted to organic chemistry.

Mechanism of nucleophilic addition

EV IE

Content

O

• formation of alkenes by elimination

students should be able to:

Section title

N

Section number

LY

Cambridge International Pre-University Chemistry

(a) use the concept of atom economy as a measure of the efficiency of use of reagents in a synthesis (expressed as a percentage using [formula weight of utilised product(s)]/ [formula weight of all the reactants used] × 100%)

Y

S

S33

S33.3

Green Chemistry

A3.6b

(b) recall and discuss measures that can reduce the impact of chemical industry and research on the environment, including: finding benign alternatives to hazardous chemicals, using renewable feedstocks, using catalysts rather than stoichiometric reagents, etc.

Y

S

S33

S33.2, S33.4

Green Chemistry

FO R

A3.6a

Original material © Cambridge University Press 2016


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