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Formation of esters (Esterification)
(1) The reaction is shifted to the right via using excess of alcohol or removal of water by distillation.
(2) The reactivity of alcohol towards esterification.
tert-alcohol < sec-alcohol < pri-alcohol < methyl alcohol
(3) The acidic strength of carboxylic acid plays just a minor role.R3CCOOH2CHCOOH2COOH3COOH
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Explain Carbocation The mechanism is a sequence of two Brønsted acid-base reactions. In the first (step a), the double bond is protonated to give a tertiary carbocation; in the
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Question: (i) Differentiate between ionic, metallic, covalent and dipole-dipole bonds. Provide examples in each case. (ii) With regard to electronic con?guration, what do a
We performed a titration in the lab with mock gastric juice and potassium hydroxide. We titrated to end point and then to another colour change and noted both the volumes. We are n
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