For each pair of compounds in questions 01.1 and 01.2, give a reagent (or combination of reagents) that could be added separately to each compound to distinguish between them. State what is observed in A and B.
A is a ketone, B is a carboxylic acid
Universal indicator
A has no change/ neutral
B is red/ acidic
Explain why more of isomer E than isomer F is formed in this reaction.
More stable carbocation formed, as secondary carbocationsmore stable than primary carbocations
How many isomers are there of C3H9N?
A 2
B 3
C 4
D 5
C
Which compound can be oxidised to form (CH3)2CHCOCH3?
A 2-methylpropan-1-ol
B 2,2-dimethylpropanol
C 2-methylbutan-2-ol
D 3-methylbutan-2-ol
D
Which species can act as a nucleophile?
A NH4+
B CH3OH
C CH4
D H+
B
Which compound could not be produced by reacting 2-bromo-3-methylbutane with sodium hydroxide?
