can someone show me how to do the work and explain it to meHomework Answers
the product is S - configuration so the product must be R configuration
here alcohol reacts with TsCl and forms the tosylate
which is good leaving group and then undergoes SN2 reaction and
forms the product
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can someone show me how to do the work and explain it to me 16. Starting...
can someone show me how to do the work and explain it to me 16. Starting...
can someone show me how to do the work and explain it to me
16. Starting with optically pure (R) or (S)-2-butanol which method below would give the best yield of the following ether? ноCH, HC CH A) (1) (R)-2-butanol + TSCI B)(1)(S)-2-butanol + TSCI C) (1) (R)-2-butanol + Na D) (1) (S)-2-butanol + Na (2) CHONa (2) CH3ONa (2) CH31 (2) CHI
can someone show me how to do the work and explain it to me 15. How would you synthesize the following compound star...
can someone show me how to do the work and explain it to me
15. How would you synthesize the following compound starting with optically pure (R) or (5)-2 HCN H,C, X CH3 A) (1) (R)-2-butanol + TSCI B) (1) (S)-2-butanol + TsCI C) (1) (S)-2-butanol + H2SO4 (heat) D) (R)-2-butanol + NaCN/DMSO (2) NaCN/DMSO (2) NaCN/DMSO (2) HBr (3) NaCN/DMSO
How would you synthesize the following compound starting with optically pure (R) or (S)-2-butanol? 8) How...
How would you synthesize the following compound starting with
optically pure (R) or (S)-2-butanol?
8) How would you synthesize the following compound starting with optically pure (R) or (S)-2-butanol? H CN НаС. CH3 A) (1) (R)-2-butanol + TSCI B) (1) (S)-2-butanolTsCI C) (1) (S)-2-butanol + H2SO4 (heat) D) (R)-2-butanol NaCN/DMSO (2) NACN/DMSO (2) NACN/DMSO (2) HBr (3) NaCN/DMSO
QUESTION 21 How would you synthesize the following compound starting with optically pure (R) or (5)-2-butanol?...
QUESTION 21 How would you synthesize the following compound starting with optically pure (R) or (5)-2-butanol? н CN HzC CH, A. (1) (S)-2-butanol + TSCI (2) NaCN/DMSO B. (1) (R)-2-butanol + TSCH (2) NacN/OMSO C(R)-2-butanol + NaCN/OMSO y ()-2-Butanol H2504 (heat) (2) HBr (3) NaCN/DMSO QUESTION 22 CHOIS
11. How would you synthesize the following compound starting with optically pure (R)-2-butanol (note: it could...
11. How would you synthesize the following compound starting with optically pure (R)-2-butanol (note: it could require multiple steps)? HCN HC CH 12. Give the product of the following reaction: СНЫBr NASH Page 2
Can someone explain this to me and show me how to do the work. 7. Identify...
Can someone explain this to me and show me how to do the
work.
7. Identify the major product(s) in the reaction of (R)-2-bromopentane with sodium cyanide in DMSO? A. (R)-2-cyanopentane (S)-2-cyanopentane racemic mixture of 2-cyanopentane trans-2-pentene
can someone show me how to do the work and explain it to me 10. What...
can someone show me how to do the work and explain it to me
10. What is the leaving group in the following reaction? CH,CHOH + HCI , CHCHCI + 0 А. ОН НО CH3CH, CI D.
can someone show me how to do this and explain this to me Organic Chemistry 21....
can someone show me how to do this and explain this to me
Organic Chemistry 21. Which of the following mechanistic steps is the most likely route for the formation of the cyclic ether shown? N&OCH3 Он CHHОН A) В) Он D)
can someone show me how to do the work and explain it to me TIEM210-W03, Fall...
can someone show me how to do the work and explain it to me
TIEM210-W03, Fall 2019 Prof. J. Fiorito 13. What is the rate limiting step in the following reaction? (CH3)3CCI + H2O - (CH);COH + HCI A) (CH3)3CCI -- (CH3)3C' + cr B) (CH3)3C + H2O - C) (CH3),C-OH + H20 - D) H0+ + cr H (CH3)3C-OH, (CH3),COH + H30 Cl + H20
Can someone explain to me how to solve these. I dont understand how these answers are correct. II. (16/100) Which struct...
Can someone explain to me how to solve these. I dont understand
how these answers are correct.
II. (16/100) Which structures represent likely products of the following reactions? Circle the letters corresponding to the structures of your choice. Each wrong answer will receive negative points. NC - ایک عام سا محلاه بعد - پوس-HC | ء Br , H2O H3CH2COH-3-2 methylene H CH H- CH, HgCCHCH CECHCH HgCHCCH CH3
can someone show me how to do the work and explain it to me
16. Starting with optically pure (R) or (S)-2-butanol which method below would give the best yield of the following ether? ноCH, HC CH A) (1) (R)-2-butanol + TSCI B)(1)(S)-2-butanol + TSCI C) (1) (R)-2-butanol + Na D) (1) (S)-2-butanol + Na (2) CHONa (2) CH3ONa (2) CH31 (2) CHI
can someone show me how to do the work and explain it to me
15. How would you synthesize the following compound starting with optically pure (R) or (5)-2 HCN H,C, X CH3 A) (1) (R)-2-butanol + TSCI B) (1) (S)-2-butanol + TsCI C) (1) (S)-2-butanol + H2SO4 (heat) D) (R)-2-butanol + NaCN/DMSO (2) NaCN/DMSO (2) NaCN/DMSO (2) HBr (3) NaCN/DMSO
How would you synthesize the following compound starting with
optically pure (R) or (S)-2-butanol?
8) How would you synthesize the following compound starting with optically pure (R) or (S)-2-butanol? H CN НаС. CH3 A) (1) (R)-2-butanol + TSCI B) (1) (S)-2-butanolTsCI C) (1) (S)-2-butanol + H2SO4 (heat) D) (R)-2-butanol NaCN/DMSO (2) NACN/DMSO (2) NACN/DMSO (2) HBr (3) NaCN/DMSO
QUESTION 21 How would you synthesize the following compound starting with optically pure (R) or (5)-2-butanol? н CN HzC CH, A. (1) (S)-2-butanol + TSCI (2) NaCN/DMSO B. (1) (R)-2-butanol + TSCH (2) NacN/OMSO C(R)-2-butanol + NaCN/OMSO y ()-2-Butanol H2504 (heat) (2) HBr (3) NaCN/DMSO QUESTION 22 CHOIS
11. How would you synthesize the following compound starting with optically pure (R)-2-butanol (note: it could require multiple steps)? HCN HC CH 12. Give the product of the following reaction: СНЫBr NASH Page 2
Can someone explain this to me and show me how to do the
work.
7. Identify the major product(s) in the reaction of (R)-2-bromopentane with sodium cyanide in DMSO? A. (R)-2-cyanopentane (S)-2-cyanopentane racemic mixture of 2-cyanopentane trans-2-pentene
can someone show me how to do the work and explain it to me
10. What is the leaving group in the following reaction? CH,CHOH + HCI , CHCHCI + 0 А. ОН НО CH3CH, CI D.
can someone show me how to do this and explain this to me
Organic Chemistry 21. Which of the following mechanistic steps is the most likely route for the formation of the cyclic ether shown? N&OCH3 Он CHHОН A) В) Он D)
can someone show me how to do the work and explain it to me
TIEM210-W03, Fall 2019 Prof. J. Fiorito 13. What is the rate limiting step in the following reaction? (CH3)3CCI + H2O - (CH);COH + HCI A) (CH3)3CCI -- (CH3)3C' + cr B) (CH3)3C + H2O - C) (CH3),C-OH + H20 - D) H0+ + cr H (CH3)3C-OH, (CH3),COH + H30 Cl + H20
Can someone explain to me how to solve these. I dont understand
how these answers are correct.
II. (16/100) Which structures represent likely products of the following reactions? Circle the letters corresponding to the structures of your choice. Each wrong answer will receive negative points. NC - ایک عام سا محلاه بعد - پوس-HC | ء Br , H2O H3CH2COH-3-2 methylene H CH H- CH, HgCCHCH CECHCH HgCHCCH CH3
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