can someone show me how to do the work and explain it to meHomework Answers
option B is the answer
Explanation: NaCN is a strong nucleophile which gives SN2 substitution reaction with alkyl halide and produces substituted product. SN2 substitution reaction is fastest in sterically less hindered substrates and slowest in sterically more hindered substrates.
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14. Which...
can someone show me how to do the work and explain it to me 8. Which...
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8. Which of the following reacts fastest with methanol by the SNI mechanism? A) CH2CH2CH2CH2CH2Br B) CH2CH2CH2CHCH3 Br C) (CH3)2CCH2CH3 Br D) (CH3)3CCH2Br
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 15. How would you synthesize the following compound star...
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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
can someone show me how to do this and explain this to me 22. In which...
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22. In which of the solvents below would the reaction shown take place at the fastest rate? CH2CH.CH.CH,CN + NaBr A. CH3CH CHCHBr + NaCN ethanol acetic acid dimethyl sulfoxide water
can someone show me how to do the work and explain it to me Which of...
can someone show me how to do the work and explain it to me
Which of the following is the rate law for the Syl mechanism of an alkyl halide with a nucleophile? rate = kalkyl halide] rate = k/nucleophile rate = kalkyl halide||nucleophile rate = k[alkyl halide nucleophile
can someone actually explain and show me how to do the work ? Organic Chemistry I...
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?
Organic Chemistry I CHEM210-wo, Fall 2019 Prof J Fiorito 6. Which halide ion reacts the fastest with cyclopentyl p-toluenesulfonate in et 073 ethanoll w en 1), B) B: C) cº D) pe
UU.CICIDI QUESTION 16 Which of the following reacts the slowest with sodium cyanide, NaCN? "OTS OTS...
UU.CICIDI QUESTION 16 Which of the following reacts the slowest with sodium cyanide, NaCN? "OTS OTS B.B QUESTION 17 which the triinuing
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 the work and explain it to me 12. Which...
can someone show me how to do the work and explain it to me
12. Which of the following does not correctly describe NZ he following does not correctly describe SN2 reactions of alkyl halides? B. Tertiary halides react faster than secondary halides. e or reaction depends on the concentrations of both the alkyl halide and the nucleophie. The mechanism consists of a single step with no intermediates. The transition state species has a penta valent carbon atom.
can someone show me how to do the work and explain it to me 12. Which...
can someone show me how to do the work and explain it to me
12. Which of the following does not correctly describe Sn2 reactions of alkyl halides? Tertiary halides react faster than secondary halides. Rate of reaction depends on the concentrations of both the alkyl halide and the nucleophile. The mechanism consists of a single step with no intermediates. The transition state species has a pentavalent carbon atom.
can someone show me how to do the work and explain it to me
8. Which of the following reacts fastest with methanol by the SNI mechanism? A) CH2CH2CH2CH2CH2Br B) CH2CH2CH2CHCH3 Br C) (CH3)2CCH2CH3 Br D) (CH3)3CCH2Br
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
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
can someone show me how to do this and explain this to me
22. In which of the solvents below would the reaction shown take place at the fastest rate? CH2CH.CH.CH,CN + NaBr A. CH3CH CHCHBr + NaCN ethanol acetic acid dimethyl sulfoxide water
can someone show me how to do the work and explain it to me
Which of the following is the rate law for the Syl mechanism of an alkyl halide with a nucleophile? rate = kalkyl halide] rate = k/nucleophile rate = kalkyl halide||nucleophile rate = k[alkyl halide nucleophile
can someone actually explain and show me how to do the work
?
Organic Chemistry I CHEM210-wo, Fall 2019 Prof J Fiorito 6. Which halide ion reacts the fastest with cyclopentyl p-toluenesulfonate in et 073 ethanoll w en 1), B) B: C) cº D) pe
UU.CICIDI QUESTION 16 Which of the following reacts the slowest with sodium cyanide, NaCN? "OTS OTS B.B QUESTION 17 which the triinuing
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 the work and explain it to me
12. Which of the following does not correctly describe NZ he following does not correctly describe SN2 reactions of alkyl halides? B. Tertiary halides react faster than secondary halides. e or reaction depends on the concentrations of both the alkyl halide and the nucleophie. The mechanism consists of a single step with no intermediates. The transition state species has a penta valent carbon atom.
can someone show me how to do the work and explain it to me
12. Which of the following does not correctly describe Sn2 reactions of alkyl halides? Tertiary halides react faster than secondary halides. Rate of reaction depends on the concentrations of both the alkyl halide and the nucleophile. The mechanism consists of a single step with no intermediates. The transition state species has a pentavalent carbon atom.
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