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- Match the questions with the correct descriptions below: Sn2, E2 E1cb Sn1, E1 (anti) E2, E1cb Sn1, E1 2 steps poor leaving group 2 carbons removed from a carbonyl group carbanion intermediate 3°>allylic, benzylic>2°>1°>CH₃ carbocation intermediate Ist order reaction (r=k[RX]) H-X anti no intermediate 2nd order reaction (r=k[RX][Nu]) polar aprotic solventA) what is the major product if E2 mechanism is followed in the reaction (A-D) B) what is the complete mechanism with steps to form the major productFill in the missing reagents a-e in the following scheme:
- Rank the following alkyl halides in term of reactivity in a E2 reaction with NaOH (fastest (1) to slowest (4)): 1-bromo-2,2-dimethylpentane, 1-chloro-2,2-dimethylpentane, 2-chloro-2-methylpentane, and 2-bromo-2-methylpentane.Rank the following E2 reactions in order of increasing rate. Show the final product.Show me the mechanism of this reaction using only 1 bromination. *R listed is NHCOCH3.
- Which of A to E shows the structure of the major product obtained from the E1 reaction shown below?Draw Sn1/E1 products of both reactions below or fill in the blank with appropriate stuffs for Sn1/E1The Hofmann product is favored by the E2 mechanism when 2-bromo-3-methylbutane is added: A. MeOH B. MeO:- in MeOH C. Nal in acetona D. (CH 3)3 CO:- in (CH 3),COH
- Why is this considered an Elimination E2 reaction? C₃H₈O (l) → C3H6 (g) + H2O (l) propan-1-ol → propene + waterSupply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2Draw the major organic product of this E1 elimination reaction. Ignore byproducts.