The first of the two heterolysis reactions below takes place readily, but the second one does not. Explain why. CH2 CI H3C H3C ECi-AI CI CI CI H3C H3C
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- For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be true for one or moremechanisms. The reaction of CH3CH2Br with NaOH occurs by this mechanism.Explain the possible mechanism (Sn1/Sn2/E1/E2) given the reaction. Show the transfer of electrons/groups, and name the product.Shown below are two reactions; Reaction 1 is a Friedel-Crafts acylation while Reaction 2 is a Friedel- Crafts alkylation. State which reaction will occur faster and justify your answer, with words and structures. Explain these all: e- density / Deactivation / Resonance stable / faster the carbonation formed because it's gonna have smaller activation energy
- Which of the following (I-III) is not a step in the mechanism of the reaction shown below.For each of the following reactions, state the mechanism the reaction will follow (E1,E2, SN1, SN2, etc.) and givethe major product(s) of the reaction.Complete all the elimination reactions/show the products, and for each reaction clearly and thoroughly explain which mechanism (E1, E2, SN1, etc.) is predominant and how it effects the product formation.
- Provide the mechanism for the conversion shown below. CH3Li is effectively H3C-Li+. What type of mechanism is occuring?For which reaction mechanisms—SN1, SN2, E1, or E2—are each of thefollowing statement true? A statement may be true for one or moremechanisms. The mechanism involves carbocation intermediates.Shown below are two reactions; Reaction 1 is a Friedel-Crafts acylation while Reaction 2 is a Friedel- Crafts alkylation. State which reaction will occur faster and justify your answer, with words and structures. Mention: e- density / Deactivation / Resonance stable / faster the carbonation formed because it's gonna have smaller activation energy
- What is the complete mechanism using curved arrow formalism of the two products shown below? Explain why one is major and the other is minor product formation.Complete the following reactions with the majority products and the missing reaction conditions. Indicate stereochemistry if applicable. Also indicate the type of reaction that took place (SN1, SN2, E1, E2, E1bc)Give the major organic product(s) for each step of the following sequence of reactions
