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vovikov84 [41]
1 year ago
7

25. 22 the reaction of phenylmagnesium bromide with methyl benzoate followed by acidification produces triphenylcarbinol. what a

re the sources of phenyl groups in triphenylcarbinol?
Chemistry
1 answer:
ExtremeBDS [4]1 year ago
3 0

Triphenylcarbinol( or triphenylmethanol) gets its phenyl groups from phenylmagnesium bromide.

Synthesis of triphenylcarbinol:

A typical laboratory experiment for demonstrating the Grignard reaction is the synthesis of triphenylmethanol using methyl benzoate, benzophenone, and phenylmagnesium bromide. Diethyl carbonate is a possible starting material.

Characteristics:

  • An organic substance is a triphenylmethanol. It is a white, crystalline substance that dissolves well in alcohol, diethyl ether, and benzene but not in water or petroleum ether. Due to the creation of a persistent "trityl" carbocation, it generates a bright yellow hue in very acidic solutions. Important dyes include several triphenylmethanol derivatives.
  • Triphenylmethanol has a core tetrahedral carbon atom, three phenyls (Ph) rings, and an alcohol group attached to it. With lengths of around 1.47Å for all three C-Ph bonds and 1.42Å for the C-O link, these connections are characteristic of sp3-sp2 carbon-carbon bonds.
  • Three neighboring phenyl groups give off specific qualities that are reflected in the alcohol's reactivity.

Learn more about triphenylmethanol here:

brainly.com/question/15089315

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