synthesis of tert butyl chloride lab report


How to prepare tert-butyl chloride?

Thus, we were able to prepare tert-butyl chloride by preforming a substitution reaction using tert-butyl alcohol and hydrochloric acid. The formation and reactivity of tert-butyl chloride are both achieved by an SN1 reaction. An SN1 reaction is a first order nucleophilic substitution which is unimolecular.

How does tert-butanol react with HCl?

tert-Butanol reacts readily with HCl and forms the corresponding tert-butyl chloride at room temperature. SN1 mechanisms are unimolecular because its slow step is unimolecular. The reaction proposed involves an initial step where the tert- butyloxonium ion is formed by protonation.

Why does tert-butyl chloride contain a tertiary alkyl halide?

This can be seen when comparing the results of the qualitative tests with the literature information. In test tubes one and two it is made clear that tert-butyl chloride contains a tertiary alkyl halide because it reacts and forms a precipitate with silver nitrate as the literature predicted.

What is arrow pushing in tert-butyl chloride?

In the preparation of tert-butyl chloride a mechanism called arrow pushing outlines the movement of elections throughout the course of a reaction to track the pacing and overall progression of the reaction.

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