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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
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter21: Nas: Nucleophilic Aromatic Substitution
Section: Chapter Questions
Problem 7E
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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
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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