M6S8 – Organic Mechanisms

10

Organic Mechanisms

1 / 10

Which statement helps to explain why propene react with hydrogen bromide to form mainly 2-bromopropane and much less 1-bromopropane?

2 / 10

Which of these chemical species are nucleophiles with react with halogenoalkanes?

(i) cyanide ions

(ii) hydroxide ions

(iii) ammonia molecules

(iv) ammonium ions

3 / 10

Which of these chemical species are electrophiles which add to alkenes?

(i) bromine molecules

(ii) sulfuric acid molecules

(iii) hydrogen bromide molecules

(iv) sulfate ions

4 / 10

In which of these reactions between pairs of reagents is the bond breaking homolytic?

(i) butan-1-ol with sodium bromide and concentrated sulfuric acid

(ii) catalytic cracking of hydrocarbons

(iii) bromine with ethene

(iv) bromine with hexane

5 / 10

In which of these reactions between pairs of reagents is the bond breaking heterolytic?

(i) hydrogen bromide with propene

(ii) hydrogen bromide and butan-1-ol

(iii) sodium hydroxide with 1-bromopropane

(iv) bromine with hexane

6 / 10

Which of these changes represents a termination step of a chain reaction?

(i) CH3. + CH3. -> CH3CH3

(ii) CH3. + Br2 -> CH3Br + Br.

(iii) Br. + Br. -> Br2

(iv) Br. + CH4 -> CH3. + HBr

7 / 10

In which of these organic compounds are all the bonds non-polar?

(i) 1-bromobutane

(ii) butene

(iii) butan-2-ol

(iv) butane

8 / 10

Which of these conversions is an example of nucleophilic substitution?

9 / 10

Which of these statements defines a free radical?

10 / 10

Methane reacts with chlorine in the presence of ultraviolet light. The reactive chemical species which attacks methane molecules during the reaction is:

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