Below is a mechanism that represents the following single reaction sequence: a certain alcohol undergoes acid- catalyzed dehydration (conversion that involves the loss of water from the reacting molecule or ion) to form an alkene product. Write the IUPAC name of the product. Include E/Z stereochemistry. Hint: Name of the substituent of the product is similar to that of reactant. * H :ÖH :0: HLösÖH 1-phenylpropanol oxonium ion H H HỘH Carbocation stabilised by resonance loss of water benzylic carbocation organic product + H-B Alkene formed proton abstraction
Below is a mechanism that represents the following single reaction sequence: a certain alcohol undergoes acid- catalyzed dehydration (conversion that involves the loss of water from the reacting molecule or ion) to form an alkene product. Write the IUPAC name of the product. Include E/Z stereochemistry. Hint: Name of the substituent of the product is similar to that of reactant. * H :ÖH :0: HLösÖH 1-phenylpropanol oxonium ion H H HỘH Carbocation stabilised by resonance loss of water benzylic carbocation organic product + H-B Alkene formed proton abstraction
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:loss of water
benzylic carbocation
organic product + H-B
Alkene formed
proton abstraction
The resonance structures
for a benzylic carbocation
Your answer

Transcribed Image Text:Below is a mechanism that represents the following single reaction
sequence: a certain alcohol undergoes acid- catalyzed dehydration
(conversion that involves the loss of water from the reacting molecule or
ion) to form an alkene product. Write the IUPAC name of the product.
Include E/Z stereochemistry. Hint: Name of the substituent of the product
is similar to that of reactant. *
:ÖH
:O:
:0:
:O:
1-phenylpropanol
oxonium ion
H.
нон
Carbocation stabilised by resonance
loss of water
benzylic carbocation
organic product + H-B
Alkene formed
;B
proton abstraction
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