Home
Class 12
CHEMISTRY
Give the structures of (A),(B) and (C)(e...

Give the structures of `(A),(B)` and `(C)(`explanation is not required `).`
`i.` `(A)(C_(4)H_(8))` that adds on `HBr` in the presence and in the absence of peroxide to give the same product, `C_(4)H_(9)Br`.
`ii.` `(B)(C_(4)H_(8)),` which when treated with `H_(2)O //H_(2)SO_(4)` gives `C_(4)H_(10)O` that cannot be resolves into optical isomers.
`iii.` `(C)(C_(6)H_(12),` an optically active hydrocarbon which on catalytic hydrogenation gives an optically inactive compound, `C_(6)H_(14))`

Promotional Banner

Similar Questions

Explore conceptually related problems

An optically active hydrocarbon X has molecular formula C_(6)H_(12) . X on catalytic hydrogenation gives optically inactive C_(6)H_(14).X could be

The number of optically active compounds in the isomers of C_(4)H_(9)Br is

Optically active isomer (A) of (C_(5)H_(9)Cl) on treatment with one mole of H_(2) gives an optically inactive compound (B) compound (A) will be :

C_(4)H_(8)O_(2) represents :-

Give the structures of the hydrocarbons corresponding to the molecular formula C_(8)H_(12)

The charing product formed when C_(6) H_(12) O_(6) is heated with cone, H_(2)SO_(4) is due to:

C_(6)H_(12)O_(6) + Ararr2C_(3)H_(4)O_(3)+ B . A & B in the above reaction are

An optically active compound H(C_(5)H_(6)O) on treatment with H_(2) in the presence of Lindlar's catalyst gave a compound I (C_(5)H_(8)O) . Upon hydrogenation with H_(2) and Pd/C, Compound H gave J (C_(5)H_(12)O) . Both I and J were found to b optically inactive. Select the correct statements.