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- Identify the mechanistic pathways, respectively, for the products in the following reaction. a) E1, SN1 b) E1, SN2 c) E2, SN1 d) E2, SN2Which of the reactions below are correctly identified? These are SN2 reactions:As measured by their first-order rate constants, the compound shown (R = CH3) undergoes hydrolysis 26 times faster than 2-chloro-2-phenylpropane (R = H) in 90% acetone–10% water at 25°C. Offer a resonance explanation for this rate difference.
- Optically active butan-2-ol racemizes in dilute acid. Propose a mechanism for this racemization.Show how the dehalogenation of (1R,2R)-1,2-dibromo-1,2-diphenyl ethane with zinc affords cis-stilbene. Show the mechanism with pictures.2. (a) Write the reaction equation of substitution reaction when 1-bromopropane reacts with(i) NaOH aqueous(ii) Excess NH3(iii) KCNb) Write the reaction mechanism for the reaction in a)(i).
- 1-Chlorobutane, CH3CH2CH2CH2Cl, reacts with aqueous sodium hydroxide by a second-order nucleophilic substitution reaction, SN2. a) Draw a diagram to show the mechanism of this reactionWhat's the mechanism for the SN2 reaction of NaI with 1-bromobutane?What is the predominant mechanism of the reaction below? SN2 SN1 E2 E1