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- Which product would likely be the major product for the following reaction?a. Ab. Cc. Dd. BConsider the series of the trans effect: CO, CN-, C2H4 > PR3, H-, CH3- > C6H5- > NO2-, SCN-, I- > Br- >Cl- > py > NH3 > H20 What would be the major product of the following reaction? Select one:In which of the reactions below does the carbocation act as an acid? 1 2 3 NONE
- Consider the attached E2 reaction What happens to the reaction rate with each of the following changes?[1] The solvent is changed to DMF. [2] The concentration of −OC(CH3)3 is decreased. [3] The base is changed to −OH. [4] The halide is changed to CH3CH2CH2CH2CH(Br)CH3. [5] The leaving group is changed to I−.Which product would likely be the major product for the following reaction?a. Bb. Cc. Ad. D2. How many substitution product/s is/are formed when metabromo anisole is treated with ammonia?A. 0-no reactionB. 1C. 2D. 3
- In each case tell which SN2 reaction will proceed faster.1. The displacement by I- on (a) CH3Cl or (b) CH3OTos. Select A or B2. The displacement by OH- on (a) CH3Br or (b) CH3I. Select A or B1. What type of reaction is occuring in step 3? (halogenation, hydrohalogenation, reduction, keto–enol tautomerism, dehydrohalogenation, acid-catalyzed hydration, base-catalyzed hydration) 2. Which reagent is necessary for step 3? (Br2, HBr, H2/Pt, NaNH2, H20/H2SO4/HgSO4)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 solvent
- What is the product of the nucleophilic substitution reaction shown below? Only I Only II I and II Nonewhat is the product for this substitution reaction belowMatch the reactant with the product of its reaction with HClO4. Leave blank if there is no reaction. Group of answer choices K2S KHCO3 HNO3 K2SO3