Question
The purpose of the experiment was to form pure triphenylmethanol through a multi-step synthesis. The first step was to convert the carboxylic acid (benzoic acid)
The purpose of the experiment was to form pure triphenylmethanol through a multi-step synthesis. The first step was to convert the carboxylic acid (benzoic acid) into the ester (methyl benzoate) through a procedure called Fischer esterification. The second step was to prepare phenyl magnesium bromide, which is a Grignard reagent and to add it to the methyl benzoate. The third step was to isolate the final product (triphenylmethanol).
The mass of methyl benzoate collected was s 7.56 g and the percent yield was 68%
The mass of Triphenyl methanol collected was 3.01 g and the percent yield was 32%
Can we use triphenylmethanol or methyl benzoate as a precursor for future experiments?
Step by Step Solution
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There are 3 Steps involved in it
Step: 1
Both benzoic acid and triphenyl are organic solutes and therefore will dissolve in organic solvents ie diethyl ether Benzoic acid an acid will react with a strong base ie NaOH to form sodium benzoate ...Get Instant Access to Expert-Tailored Solutions
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Step: 2
Step: 3
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