can someone show me how to do this and explain this to me 0 IUINU nations...
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 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 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 show me how to do the work and explain it to me 9. A pentacoordinate carbon is a transient species in the mechanism. SNI SN2 EI E2 C. D.
Multiple Choice Identify the choice thar best completes the statement or answers the question. Use the alkyl bromides below to answer the following five questions: Br -Br CH3 Br IV 10. Which of the alkyl halides is most likely to participate in an SN2 reaction? a. II d. III b. IV e. V c. I 11. Compound II can be classified as a alkyl halide. e. I a. quaternary c. primary b. tertiary d. secondary 12. Which of the alkyl...
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 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
1. Which of the following structures is/are a secondary alkyl halide? (a) I and II (b) II and V (c) I, II and V (d) IV only (e) I, II and III 2. Which of the following is/are aprotic solvent(s)? Choose all correct answers. (a) (b) (c) (d) (e) (f) 3. Which of the following carbocations, if formed, is (are) likely to undergo rearrangement through a hydride shift? (a) I (b) II (c) III (d) I and II (e) II...
CIC-CH.CH $$ 0,09 ( -CCHCH, K CANON D) IV 2, whicen er falowing the A) B) II CITI 21) Which of the following alkenes is the most stable? or more com B) II D) IV 22) For the following reaction, use the identity of the alkyl halide and nucleophile to determine which substitution mechanism occurs. Then determine which solvent affords the faster reaction. OH + BO • ное но A) SN 2, H20 B DMF ) SN1, H20 SN1, DMF...
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.