The ozonolysis reactions used to as cert...

The ozonolysis reactions used to as certain the position of multiple bonds in a substrate. The most widely used ozonolysis is partial reductive ozonlysis, which is also used for preparation of aldehyde and ketones.

An unsaturate Hydrocarbon (A) C.Hreadily gives (B) on treatment with NaNH, with 1-chloropane, C is obtained on partial hydrogenation with Lindaar's catalyst C gives D. On ozonolysis, (D) gives 2,2-dimethyl propanal and 1-butanal.
A is

`CH_3CH_2 - underset(CH_3)underset(|)overset(CH_3)overset(|)C-C -=CH`

`CH_3-underset(CH_3)underset(|)overset(CH_3)overset(|)C-C-=CH`

`CH_3-underset(CH_3)underset(|)overset(CH_3)overset(|)-CH=CH_2`

`CH_3-underset(CH_3)underset(|)overset(CH_3)overset(|)C-CH=C=CH_2 `

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The correct Answer is:

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Ethylene on ozonolysis gives

Formaldehyde

Ethylene ozonide

Acetaldehyde

`H_(2)O_(2)`

4-oxopentanal

3-oxopentanal

Hexane-2, 5-diene

Pentanedial

`underset(H-C=O)underset(|)(H-C=O)`

`H-underset(H)underset(|)(C)=O`

`CH_(3)-underset(H)underset(|)(C)=O`