A secondary butyl free radical is more stable than the primary butyl free radical. It is due to the

(B) the steric effect of the tert-butyl group. The steric hindrance caused by bulky tert-butyl group results in monosubstitution form heavier iodine and trisubstitution of lighter chlorine. (C) the electronic effect of the phenolic group.

Arrange the following alcohols in the decreasing order of their boiling points. 1. n-Butyl alcohol 2. sec-Butyl alcohol

A tertiary butyl carbocation is more stable than a secondary butyl carbocation because of which of the following ? <!--td {border: 1px solid #cccccc;}br {mso-data-placement:same-cell;}--> NEET 2020 View Solution

When a hydrogen is removed from butane, butyl group is obtained. Hence, the structure of 3-methylbutyl group is obtained, when one hydrogen atom is removed from 3-methylbutane. i.e. C H 3 − C H | C H 3 C H 2 C H 3 after removing one hydrogen ( C H 3 ) 2 C H C H 2 C H 2 −

Statement A: When the ring contains more or equal number of carbon atoms than the alkyl group attached to it, then it is named as a derivative of cyclo alkane and the alkyl group is treated as substituent.

Tert-butyl group is named as: 1, 1 ... The common name of the group, (C H 3) 2 C H C H 2 ...

In the following reaction, the steric of the tetra-butyl group which is attached to the benzene ring. That is why, the reactivity of compound Z with different halogens under appropriate condition and electro-negativity of the halogens is C l 2 > B r 2 > I 2.

211.Iso-butyl bromide reacts with aq. KOH gives 1.iso-butyl alcohol 2.t-butyl alcohol 3.n-butyl alcohol 4.sec-butyl alcohol CORRECT ANS IS 2.

Click here:point_up_2:to get an answer to your question :writing_hand:the structure of isobutyl group is an organic compound is