1. Draw the two-step reagent sequence which accomplishes the anti-Markovnikov hydration of an alkyne. Also draw the product of anti-Mark hydration of 1-propyne, as well as the complete arrow-pushing mechanism of its formation (use "R"s for the reagent only in your mechanism). The mechanism is mostly the exact same as the similar reaction on an alkene, except for the end. Offer a brief explanation of why this mechanism results in an anti-Markovnikov addition. H3C =-H

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1. Draw the two-step reagent sequence which accomplishes the anti-Markovnikov hydration of
an alkyne. Also draw the product of anti-Mark hydration of 1-propyne, as well as the complete
arrow-pushing mechanism of its formation (use “R"s for the reagent only in your mechanism).
The mechanism is mostly the exact same as the similar reaction on an alkene, except for the end.
Offer a brief explanation of why this mechanism results in an anti-Markovnikov addition.
H,C–=H
Transcribed Image Text:1. Draw the two-step reagent sequence which accomplishes the anti-Markovnikov hydration of an alkyne. Also draw the product of anti-Mark hydration of 1-propyne, as well as the complete arrow-pushing mechanism of its formation (use “R"s for the reagent only in your mechanism). The mechanism is mostly the exact same as the similar reaction on an alkene, except for the end. Offer a brief explanation of why this mechanism results in an anti-Markovnikov addition. H,C–=H
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