The product of reductive hydrolysis of ozonide of 1-butene are:

Ethanal only

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Ethanal and methanal

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Propanal and methanal

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Methanal only

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Solution

The correct option is C Propanal and methanal

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Q. Hydrolysis of ozonide of 1-butene gives:

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:

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 decompose either by reduction or hydrolysis and forms compound having. This $> C = O$ is known as ozonolysis.

Product P is

Q. The major products obtained during ozonolysis of

2, 3 - d i m e t h y l - 1 - b u t e n e

and subsequent reductions with

Z n

and

H_{2} O

are :

Q. Assertion :Ozonolysis of 3-hexyne followed by hydrolysis gives propanoic acid. Reason: The byproduct

H_{2} O_{2}

oxidizes ozonide to acid.

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