5. A student attempted the following Mizoroki-Heck reaction, expecting to get product A which contains a double bond. To their surprise, product B was found instead, which contains no carbon-carbon bond. Draw the key mechanistic steps that explain what happened. OH [Pd] NEt3 OH not observed میل B only product

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5. A student attempted the following Mizoroki-Heck reaction, expecting to get product A
which contains a double bond. To their surprise, product B was found instead, which
contains no carbon-carbon bond. Draw the key mechanistic steps that explain what
happened.
OH
OH
obro do
A
not observed
[Pd]
NEt3
B
only product
Transcribed Image Text:5. A student attempted the following Mizoroki-Heck reaction, expecting to get product A which contains a double bond. To their surprise, product B was found instead, which contains no carbon-carbon bond. Draw the key mechanistic steps that explain what happened. OH OH obro do A not observed [Pd] NEt3 B only product
Expert Solution
Step 1: Describe Mizoroki-Heck reaction

The Mizoroki-Heck reaction is a palladium-catalyzed coupling reaction between an alkene (containing a carbon-carbon double bond) and an aryl or vinyl halide to form a new carbon-carbon bond. It's important to understand the mechanism to explain why the student obtained product B, which does not contain a carbon-carbon double bond.

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