Question 1
Propanone has a much higher boiling temperature than butane.
The main reason for this is
propanone has permanent dipole-dipole forces between its molecules while butane does not
propanone forms hydrogen bonds between its molecules while butane does not
propanone has stronger induced dipole-dipole forces between its molecules than butane
the carbon-oxygen double bond in propanone is very strong
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Question 2
CH3CH2COCH2CH3 reacts with hydrogen cyanide to form an organic product called a cyanohydrin.
Which feature applies to the cyanohydrin product?
it has one chiral centre
it is formed by electrophilic addition
it is formed via an intermediate which contains the C-OH group
its formation requires the use of cyanide ions as a catalyst
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Question 3
Compound X contains two functional groups.
Which reagent will react with only one of the functional groups?
acidified potassium dichromate(VI)
2,4-DNPH reagent
hydrogen cyanide
NaBH4
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Question 4
Structural isomerism and stereoisomerism should be considered when answering this question.
Each of the following carbonyl compounds is reacted with NaBH4. The product of each reaction is heated with concentrated phosphoric acid at 170°C, generating one product or a mixture of isomers.
Which carbonyl compound will produce the most isomers?
butanal
butanone
pentan-3-one
propanone
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Question 5
Ketones react with hydrogen cyanide, HCN, in the presence of cyanide ions, CN-.
This type of reaction is classified as
nucleophilic substitution
nucleophilic addition
electrophilic addition
electrophilic substitution
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Question 6
Name the functional group in HCHO.
aldehyde
ketone
alcohol
carboxylic acid
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Question 7
What is the functional group in C6H5COCH3?
aldehyde
carboxylic acid
ester
ketone
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Question 8
Which alcohol could not be produced by the reduction of an aldehyde or a ketone?
2,2-dimethylpropan-1-ol
2-methylbutan-2-ol
3-methylbutan-2-ol
pentan-3-ol
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Question 9
Which compound forms optically active compounds on reduction?
CH3CH2C(CH3)=CHCH3
CH3CH2C(CH3)=CH2
CH3COCH3
CH3CH2COCH3
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