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    mynknaruka
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    1. A process is described for the acylation of aniline with a stronger base like pyridine added to remove the HX byproduct and shift the equilibrium in the forward direction. 2. Cyclohexylamine is more basic due to the +I effect of the cyclohexyl group, which donates electron density to the nitrogen atom. 3. Haloalkanes do not undergo nucleophilic substitution reactions.

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    1. A process is described for the acylation of aniline with a stronger base like pyridine added to remove the HX byproduct and shift the equilibrium in the forward direction. 2. Cyclohexylamine is more basic due to the +I effect of the cyclohexyl group, which donates electron density to the nitrogen atom. 3. Haloalkanes do not undergo nucleophilic substitution reactions.

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    6 views3 pages

    Rough 1

    Uploaded by

    mynknaruka
    1. A process is described for the acylation of aniline with a stronger base like pyridine added to remove the HX byproduct and shift the equilibrium in the forward direction. 2. Cyclohexylamine is more basic due to the +I effect of the cyclohexyl group, which donates electron density to the nitrogen atom. 3. Haloalkanes do not undergo nucleophilic substitution reactions.

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    © All Rights Reserved
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    of 3

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