One mole of alkene on ozonolysis gives $2$ moles of butanone. The alkene is:

3, 4-dimethylhex-2-ene

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2, 3-dimethylhex-3-ene

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3, 4-dimethylhex-3-ene

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2, 3-dimethylhex-2-ene

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2, 5-dimethylhex-3-ene

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Solution

The correct option is E 3, 4-dimethylhex-3-ene
Hence, the option $C$ is an answer.

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Similar questions

Q. Draw the structures for geometrical isomers of

3, 4 -

dimethylhex

- 3 -

ene.

Q. Which of the follwing is the correct product?

1) 3-methyl hex-2-ene

2) 3-methyl hex-3-ene

3) 3-methyl hex-3-ol

An alkene gives two moles of $H C H O$ , one mole of $C O_{2}$ and one mole of on ozonolysis follows by hydrolysis. The structure of this alkene is:

Ozonolysis of alkenes gives ozonide which gives aldehydes and/or ketones. When a stream of $O_{3}$ is passed through a solution of alkene in an inert solvent at low temperature, the molecule adds up to form ozonide. This ozonide is unstable and easily decomposes either by reduction or hydrolysis and forms compound having the carbonyl group $> C = O$ . This is known as ozonolysis. 2-Methyl-but-2-ene on ozonolysis followed by reductive hydrolysis gives:

Q. One mole of a symmetrical alkene on ozonolysis gives two moles of an aldehyde having a molecular mass of

44 u

. The alkene is:

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One mole of alkene on ozonolysis gives 2 moles of butanone. The alkene is:

The correct option is E 3, 4-dimethylhex-3-eneHence, the option C is an answer.

One mole of alkene on ozonolysis gives $2$ moles of butanone. The alkene is:

The correct option is E 3, 4-dimethylhex-3-ene
Hence, the option $C$ is an answer.