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Chapter 8: Q75P (page 377)

Which loses a proton more readily: a methyl group bonded to cyclohexane or a methyl group bonded to benzene?

Short Answer

Expert verified

The methyl group on benzene can lose a proton easier than the methyl group on cyclohexane.

Step by step solution

01

Reason behind this

The methyl group on benzene can lose a proton easier than the methyl group on cyclohexane because the electrons left behind on the carbon in the former can be delocalised into the benzene ring. In contrast, the electrons left behind in the other compound cannot be delocalised.

02

Final answer

The methyl group on benzene can lose a proton easier than the methyl group on cyclohexane.

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Most popular questions from this chapter

What is the major product of each of the following reactions? Assume that there is an equivalent amount of each reagent.

Draw the resonance contributors for the following carbocation

a. Which of the following compounds have delocalized electrons?

b. Draw the resonance contributors for the compounds that have delocalized electrons.

1.CH2=CHCH2CH=CH2

2.CH3CH=CHCH=CHCH2

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