Cyclohexene on ozonolysis followed by reaction with zinc dust and water gives compound E. Compound E on further treatment with aqueous KOH yields compound F. The compound F is:

Right on! Give the BNAT exam to get a 100% scholarship for BYJUS courses

No worries! We‘ve got your back. Try BYJU‘S free classes today!

Open in App

Solution

The correct option is A

In the first step, ozonolysis of cyclohexene is followed by reduction with zinc. We get the dicarbonyl 1,6-hexanedial.
The next step involves intramolecular Aldol addition-elimination to gives us the α-β unsaturated aldehyde. Thus we get:

Suggest Corrections

Similar questions

Q. Cyclohexene on ozonolysis followed by reaction with zinc dust and water gives compound

X

. Compound

X

on further treatment with aqueous

K O H

yields compound

Y

. Compound

Y

is:

Cyclohexene on ozonolysis followed by reaction with zinc dust and water gives compound E. Compound E on further treatment with aqueous KOH yields compound F. The compound F is:

Q. Cyclohexene on reductive ozonolysis gives compound

E

. Compound

E

on further treatment with aqueous

K O H / Δ

yields compound

F

. Compound

F

is:

Cyclohexene on reductive ozonolysis gives compound B. Compound 'B' on further treatment with aqueous NaOH followed by heating yields compound 'C'. The compound 'C' is:

Cyclohexene on reductive ozonalysis gives compound B. Compound ‘B’ on further treatment with aqueous NaOH followed by heating yields compound ‘C’. The compound ‘C’ is;

Join BYJU'S Learning Program

Explore more

Standard XIII Chemistry

Join BYJU'S Learning Program

Cyclohexene on ozonolysis followed by reaction with zinc dust and water gives compound E. Compound E on further treatment with aqueous KOH yields compound F. The compound F is:

The correct option is A In the first step, ozonolysis of cyclohexene is followed by reduction with zinc. We get the dicarbonyl 1,6-hexanedial. The next step involves intramolecular Aldol addition-elimination to gives us the α-β unsaturated aldehyde. Thus we get:

The correct option is A

In the first step, ozonolysis of cyclohexene is followed by reduction with zinc. We get the dicarbonyl 1,6-hexanedial.
The next step involves intramolecular Aldol addition-elimination to gives us the α-β unsaturated aldehyde. Thus we get: