How many rings are in X? How many double bonds are in X? Show your work. 8. continued Compound X, C37H54BT4, reacts with excess H2/Pd to give a C37H62Br4 compound.
How many rings are in X? How many double bonds are in X? Show your work. 8. continued Compound X, C37H54BT4, reacts with excess H2/Pd to give a C37H62Br4 compound.
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter14: Elimination
Section: Chapter Questions
Problem 20E
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![8. continued
Compound X, C37H54Br4, reacts with excess H2/Pd to give a C37He2Br4 compound
How many rings are in X? How many double bonds are in X? Show your work
Br
KOH
9. Write out the mechanism for:
Hi
10. For the following, use ONLY reactions we have studied in class.
a) Write out 6 completely different reactions of 2-pentanone (reagent, product).
b) Write out 3 preparations of 1-hexanol, a different starting material for each one.
You may use preps where you just change the functional group, and/or preps
where you have to construct the carbon chain.
c) Write out 3 preparations of 2-ethoxylbutanoic acid, a different starting
material for each one. You may use preps where you just change the functional
group, and/or preps where you have to construct the carbon chain.
11. Consider this list of compounds:
CH, ČCE, CH,
CH C
C,HCH
CH, C N
C,H,CN
CH,OH
C,HCOOH
CH, COOH
C,H,OCH,
CH, CH,COOH
CH,C
CH, &oCH, CH,
CH,CH,C,H,
CH, CH,OCH,CH,
CH, CHCH,
CH,CH,OH
Which ONE of them is responsible for this IR and this NMR spectrum?
IR SPECTRUM
NMR SPECTRUM
1600 1400
R.PHASE
liquid film
NMR SOLVENT
CCA](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F2acd1a8d-4262-4744-b59c-97c60e218c22%2F7464ddca-040c-4d50-915a-2ddb7b3bc1f0%2Fft2td5u_processed.jpeg&w=3840&q=75)
Transcribed Image Text:8. continued
Compound X, C37H54Br4, reacts with excess H2/Pd to give a C37He2Br4 compound
How many rings are in X? How many double bonds are in X? Show your work
Br
KOH
9. Write out the mechanism for:
Hi
10. For the following, use ONLY reactions we have studied in class.
a) Write out 6 completely different reactions of 2-pentanone (reagent, product).
b) Write out 3 preparations of 1-hexanol, a different starting material for each one.
You may use preps where you just change the functional group, and/or preps
where you have to construct the carbon chain.
c) Write out 3 preparations of 2-ethoxylbutanoic acid, a different starting
material for each one. You may use preps where you just change the functional
group, and/or preps where you have to construct the carbon chain.
11. Consider this list of compounds:
CH, ČCE, CH,
CH C
C,HCH
CH, C N
C,H,CN
CH,OH
C,HCOOH
CH, COOH
C,H,OCH,
CH, CH,COOH
CH,C
CH, &oCH, CH,
CH,CH,C,H,
CH, CH,OCH,CH,
CH, CHCH,
CH,CH,OH
Which ONE of them is responsible for this IR and this NMR spectrum?
IR SPECTRUM
NMR SPECTRUM
1600 1400
R.PHASE
liquid film
NMR SOLVENT
CCA
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