Explain the
`overset(* )CH_3` is more reactive than `CH_3 CH_2` free radical.

Explain why (CH_(3))_(3)overset(+)C is more stable than CH_(3)overset(+)CH_(2) and CH_(3) is the least stable cation

Explain the following : (a) Why MeNH overset (oplus) CH_2 (I) is more stable more than MeCH_2 overset (oplus) CH_2 (II) when both are 1^@ carbocations ? (b) Which of the following intermediate is unstable ? ( c) Why allylic free radical (CH_2 - CH = CH_2) (I) is more stable than propy1 free radical (dot C H_2 - CH_2 - CH_3) (II) , when both are 1^@ free radicals ?

Arrange the following in the order as mentioned : overset(+ )CH_3 CH_3 overset(+)CH_2, (CH_3)_2 CHoverset(+), (CH_3)_3 + C carbocations in the order of increasing reactivity,

Write the IUPAC names of the following compounds : CH_3 - overset(CH_3) overset(|) CH - CH_2 - CH_2 - overset(O ) overset( ||)C-CH_2 Cl

Explain the mechanism of the reaction is given below : 2CH_3-CH_2-OHunderset(413K)overset(H^+)to CH_3CH_2-O-CH_2-CH_3+H_2O

Which one of the following compounds is more reactive towards S_(N)2 reaction and why ? CH_3CH(Cl) CH_2CH_3 or CH_3CH_2CH_2Cl

A: CH_(3)-CH-CH_(3) has 6. hyperconjugative hydrogens while CH_(3)-CH-CH_(2) -CH_(3) has 5 hyperconjugative hydrogens. R: CH_(3)-CH-CH_(3) is more stable than CH_(3)-CH-CH_(2)- CH_3

In iso-pentane, the H atom that can be most easily substituated by free radical mechanism is on:- overset(1)CH_(3)-underset(CH_(3))underset(|)overset(2)CH-overset(3)CH_(2)overset(4)CH_(3)