Refer to the folowing reaction mechanism slow fast CH-C OCH, OH CH C-OCH OH CH-C-OH CH,0 fast CH,C-O CH,OH The least stoble transition state hos which structure? 8- A CH-C-OCH3 B. CH, C OCH, C.CH,-C-OCH, D. CH, C,OCH, OH OH OH Tme left 037 Refer to the following reaction mechanism slow CHy-C-OCH fast • OH CH,0 fast -CH,C-O CH,OH The most stable intermediate is A CH,-C oCH, B.CH, C-oCH, C. CH, C-oOH D.CH,-C-O OH Am Plane onger bo on pybecouse 14 Pyridine is a stronger base than pyerole because H. out of pyridine 1H-pyrrole lone pair in pyridine is locolized. lone pair in pyttole is locoled nerogen in pytidine is sp hybridirea nitrogen in pymole is sp hybndiced 35 the reoction beiw is on ompie of whot type of oegonic reaction? nitrogen in pyrrole is sp' hybridized. The reaction below is an example of what type of organic reaction? H2C=CH2 Br/CC4 BRCH,CH Br +] OElectrophilic Substitution ONucleophilic Substitution O Bimination Nucleophilic Addition Electrophilic Addition
Refer to the folowing reaction mechanism slow fast CH-C OCH, OH CH C-OCH OH CH-C-OH CH,0 fast CH,C-O CH,OH The least stoble transition state hos which structure? 8- A CH-C-OCH3 B. CH, C OCH, C.CH,-C-OCH, D. CH, C,OCH, OH OH OH Tme left 037 Refer to the following reaction mechanism slow CHy-C-OCH fast • OH CH,0 fast -CH,C-O CH,OH The most stable intermediate is A CH,-C oCH, B.CH, C-oCH, C. CH, C-oOH D.CH,-C-O OH Am Plane onger bo on pybecouse 14 Pyridine is a stronger base than pyerole because H. out of pyridine 1H-pyrrole lone pair in pyridine is locolized. lone pair in pyttole is locoled nerogen in pytidine is sp hybridirea nitrogen in pymole is sp hybndiced 35 the reoction beiw is on ompie of whot type of oegonic reaction? nitrogen in pyrrole is sp' hybridized. The reaction below is an example of what type of organic reaction? H2C=CH2 Br/CC4 BRCH,CH Br +] OElectrophilic Substitution ONucleophilic Substitution O Bimination Nucleophilic Addition Electrophilic Addition
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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Question
![Refer to the folowing reaction mechanism:
O'
CH3-C OCH, OH
slow
CH, C-OCH
fast
CH,-C-OH CH,0
OH
fast
CH,C O CH,OH
The least stoble transition state hos which structure?
A CH-C-OCH, B. CH, C OCH, C. CH,-C-OCH, D. CH, COCH,
OH
OH
ansaer
Tme let 037
Refer to the tollowing reaction mechanium
CH, coC,
fast
• OH CH C-OCH
slow
Нс он * сно
fast
CH,C-O CH,OH
The most stable intermediate is
A CH C осн, в сн, с осн, с. сн
C.CH, C-OH D.CH-C-0
OH
han songerto conp becouse
on 14
Pyridine is a stronger base than pyerole because
ered
H.
d out of
eon
pyridine
1H-pyrrole
ione pair in pyridine is locolized.
lone poir in pyrtole in locakzed
Nrogan in pytidine is sp hybridirea
ntrogen in pymole is sp'nybndced
15
the seoction eiow is on omple of whot hpe of oegoriC eaction?
O nitrogen in pyrrole is sp hybridized.
The reaction below is an example of what type of organic reaction?
H2C=CH2
Br/CC4
BRCH,CH,Br
+1
OElectrophilic Substitution
CNucleophilic Substitution
O Bimination
ONucleophilic Addition
Electrophilic Addition](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fbf41732d-9b6c-48e3-b5ea-1f1b6c8ddb16%2F51f62d03-cb98-4ca9-b933-b4c7b26bab3f%2Fzgy7i85_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Refer to the folowing reaction mechanism:
O'
CH3-C OCH, OH
slow
CH, C-OCH
fast
CH,-C-OH CH,0
OH
fast
CH,C O CH,OH
The least stoble transition state hos which structure?
A CH-C-OCH, B. CH, C OCH, C. CH,-C-OCH, D. CH, COCH,
OH
OH
ansaer
Tme let 037
Refer to the tollowing reaction mechanium
CH, coC,
fast
• OH CH C-OCH
slow
Нс он * сно
fast
CH,C-O CH,OH
The most stable intermediate is
A CH C осн, в сн, с осн, с. сн
C.CH, C-OH D.CH-C-0
OH
han songerto conp becouse
on 14
Pyridine is a stronger base than pyerole because
ered
H.
d out of
eon
pyridine
1H-pyrrole
ione pair in pyridine is locolized.
lone poir in pyrtole in locakzed
Nrogan in pytidine is sp hybridirea
ntrogen in pymole is sp'nybndced
15
the seoction eiow is on omple of whot hpe of oegoriC eaction?
O nitrogen in pyrrole is sp hybridized.
The reaction below is an example of what type of organic reaction?
H2C=CH2
Br/CC4
BRCH,CH,Br
+1
OElectrophilic Substitution
CNucleophilic Substitution
O Bimination
ONucleophilic Addition
Electrophilic Addition
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