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A: Solution 40: option A is correct.
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- Rank the following from most reactive to least reactive in an SN1 reaction.Order the compounds from most to least reactive in SN2 reactions. Explain why.5. Predict whether each reaction will occur via SN2 or E2 mechanism and draw the product. Write 'NR' if the reaction will not proceed as written. & CH3CI NaCl Acetone KOt-Bu t-BuOH KOt-Bu t-BuOH NaOEt EtOH
- ?Which of the following is not a nucleophile اخترأحد الخیارات а. NH3 -b. Br c. FeBr3 d. CH30CH3Which of these will be the most likely to rearrange during an SN1 reaction. TsO Br BrIn an E2 mediated elimination reaction of an alkyl halide (H-X) using NaOCH3 as base, which of the following statement is not true? O The reactivity order for alkyl halides (RX) is tertiary secondary> primary. O The rate of reaction = k2 (alkyl halide] [NaOCH₂] O The reaction occurs in a single step. O The rate is independent of the leaving group.
- 4. Which one of the following compounds will react faster by SN1? PhBr PhCH2Br PHCH= CHBr MezCBr Ph:CBr A EHow do you properly write an SN1 reaction, with transition states/intermediate steps included?What is the rate-determining step in the mechanism of an electrophilic substitution reaction of benzene? Select one: OA. Attachment of the electrophile to benzene ring. OB. Bonding of catalyst to electrophile precursor. O C. Reformation of acid catalyst. OD. Formation of the electrophile. OE. Loss of H+ ion form arenium ion intermediate to reform aromatic ring.
- For the given SN2 reaction, draw the organic and inorganic products of the reaction, and identify the nucleophile, substrate, and leaving group. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Hmm.. CEN + CI Organic product Inorganic productWhich rearrangement would the two example of carbocation below most likely undergo? a. Methyl shiftb. Hydride shiftc. Paradigm shiftd. Equilibrium shiftWhen Is the Reaction SN1, SN2, E1, or E2?