$O_{3}$ does not give ozonide with :

2-Butene

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Benzene

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2-Pentyne

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Neopentane

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Solution

The correct option is C Neopentane
$O_{3}$ gives ozonide with organic compounds having double or triple bonds. Neopentane only has single bonds so $O_{3}$ does not give ozonide with it.

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Similar questions

Q. A hydrocarbon X on treatement with

O_{3}

followed by the reduction of ozonide with

Z n - H_{2}

O gives Y. Y gives both Tollen's test as well as yellow precipitate with

N a O H / I_{2}

solution. Which is a possible structure of X?

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

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. Hydrolysis of ozonide of 1-butene gives:

O_{3}

does not oxidise:

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O3 does not give ozonide with :

The correct option is C NeopentaneO3 gives ozonide with organic compounds having double or triple bonds. Neopentane only has single bonds so O3 does not give ozonide with it.

$O_{3}$ does not give ozonide with :

The correct option is C Neopentane
$O_{3}$ gives ozonide with organic compounds having double or triple bonds. Neopentane only has single bonds so $O_{3}$ does not give ozonide with it.