The most reactive amine towards dilute hydrochloric acid is ___________.
•
being the strongest base among the given alkyl amines and interacts far better than towards dilute hydrochloric acid.
Reason being the presence of the 2 –CH3 groups on the adjacent carbon atoms which is more than (i) CH3—NH2 as the electron releasing + I effect pushes electron more effectively to N atom in case of
.
• But the case of
is contradictory because of steric factors. The N atom is surrounded by 3 bulky methyl groups which increases the chance for HCL protons to interact and bind to the unshared electron pairs on N atom, therefore, protonation is less effective here.
•
being the least basic(conjugation of amino group with benzene ring) will be the least reactive towards HCL.
Couldn't generate an explanation.
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