An alkene on reductive ozonolysis gives two products A and B. When these products are treated with conc. KOH one of these products gives an alcohol and an acid salt. Here the alkene can be

Question

An alkene on reductive ozonolysis gives two products A and B. When these products are treated with conc. KOH one of these products gives an alcohol and an acid salt. Here the alkene can be (A) But-2-ene (B) Pent-2-ene (C) Isobutene (D) cyclo hexene

Tardigrade Admin · Accepted Answer

Here alkene is isobutene and the reactions are as follows <img class="img-fluid question-image" alt="Solution" src="https://cdn.tardigrade.in/q/nta/c-tr7i17be9bde.png" /> As formaldehyde on heating with conc. KOH gives CH3OH and HCOOK. HCHO overset overset-O H arrow CH3OH+HCOO-

Q. An alkene on reductive ozonolysis gives two products A and B. When these products are treated with conc. KOH one of these products gives an alcohol and an acid salt. Here the alkene can be

But-2-ene

Pent-2-ene

Isobutene

cyclo hexene

Here alkene is isobutene and the reactions are as follows

As formaldehyde on heating with conc. KOH gives $C H_{3} O H$ and HCOOK.

$H C H O \to O - H C H_{3} O H + H CO O^{-}$

Q. An alkene on reductive ozonolysis gives two products A and B. When these products are treated with conc. KOH one of these products gives an alcohol and an acid salt. Here the alkene can be

But-2-ene

Pent-2-ene

Isobutene

cyclo hexene

Here alkene is isobutene and the reactions are as follows As formaldehyde on heating with conc. KOH gives CH3​OH and HCOOK. HCHO→O−HCH3​OH+HCOO−

Here alkene is isobutene and the reactions are as follows

As formaldehyde on heating with conc. KOH gives $C H_{3} O H$ and HCOOK.

$H C H O \to O - H C H_{3} O H + H CO O^{-}$