option B is correct
Explanation: protonation of alcohol with HCl gives a good leaving group, H2O which on dissociation from alcohol produces carbocation as an intermediate which on further reaction with chloride ion produces alkyl chloride as product.
can someone show me how to do the work and explain it to me 10. What...
can someone explain this to me and actually show me how to do the work ? 10. What is the leaving group in the following reaction? СНСЬCI + њо СНЫСЊOH + HCI ОН Н,0 CH3CH, СІ
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 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 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 14. Which of the following reacts the slowest with sodium cyanide, NACN? OTs A) OTs B) D) OTs OTs
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 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 th following ether? ноCH, HC CH, A) (1) (R)-2-butanol + TSCI B)(1)(S)-2-butanol + TSCI C) (D) (R)-2-butanol + Na D) (1) (S)-2-butanol + Na (2) CHONa (2) CHONa (2) CH31 (2) CH31
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 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 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.