Uploaded November 2021 | Updated September 2026, 1 week ago
The mechanism for the protection of an amine using a Troc protecting group. 2,2,2-Trichloroethoxycarbonyl (Troc) group is a commonly used carbamate protecting group for amines. It is also used to protect alcohols and phenols. Troc group is stable under hydrolytic, strongly acidic, nucleophilic, and mild reductive conditions. It can be deprotected under single electron reduction conditions using zinc-acetic acid
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The mechanism for the protection of an amine using a Troc protecting group. 2,2,2-Trichloroethoxycarbonyl (Troc) group is a commonly used carbamate protecting group for amines. It is also used to protect alcohols and phenols. Troc group is stable under hydrolytic, strongly acidic, nucleophilic, and mild reductive conditions. It can be deprotected under single electron reduction conditions using zinc-acetic acid
Music: Graffiti – Mokka






![Brook Rearrangement Mechanism | Organic Chemistry
Rearrangement of α-silyl oxyanions to α-silyloxy carbanions via a reversible process involving a pentacoordinate silicon intermediate is known as the [1,2]- Brook rearrangement, or [1,2]-silyl migration.
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