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

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 −

(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

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.

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.

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

>>Organic Chemistry - Some Basic Principles and Techniques. Nomenclature of Organic Compounds >> The IUPAC name of the t - butyl group is The IUPAC name of the t - butyl group is

butyl is a four- carbon alkyl radical-C4H9, derived from either of the two isomer of butane. The terms primary, secondary , tertiary and quaternary refer to a carbon attached to one, two, three, or four other carbons respectively. Isobutyl group is a PRIMARY alkyl group.

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