Consider the reaction and answer the questions that follow. CH-CH,-CH,-I + CHS° CH-CH,-CH,-S-CH; + CH3- CH= CH2 Product A Product B I Explain which type or types of mechanisms (S1. S2. E1, and E2) are applicable to this reaction. O How can you increase the percentage of Product A? How can you obtain Product B as almost the only product?

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What is the structure of product 2 in the reaction sequence shown below? a) b c) e) •NH₂ 01 CH₂ Nit ₂ CH2NH NH ₂ N₁ NO₂ X НСI NO₂ масл эу H₂ 72 Ni

What product do you expect from the reaction shown?

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What is most likely the first step of this reaction's mechanism? CH3 CH;CH,OH Br Br CH3CH2O -H- CH3 Br CH3CH2OH

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A. Identify the major and minor product(s) of the following reaction: Major product(s): OH 2 2 2 2 2 eTextbook and Media Minor product(s): OH 122923 NaOEt B. Add curved arrow(s) to draw step 1 of the mechanism. Modify the given drawing of the product as needed to show the intermediate that is formed in this step. се CH, + -CH, OH Edit Drawing CH₂ CH₂ OH C. Predict which of the following substrates will undergo a solvolysis reaction more quickly. Explain your choice. This compound is expected to undergo solvolysis more rapidly because it will proceed via a that is D. Identify the reagent(s) (A - I) you would use to accomplish each of the following transformations. For transformations that require more than one reagent, enter all reagents in the order they should be introduced separated by a comma (e.g. "BA"). DO NOT INCLUDE SPACES BETWEEN LETTERS. A: HBr B: "OH C: HCI D: TsCl, pyridine E: "CN F: "SH G: CH3COO H: H₂O 1: H₂S (c) Reagent(s): (d) Reagent(s): Br OH

Fill in the lettered reagents (A-G) in the following reaction scheme. CHO HO COOH C. HO C CH (1) A (2) H,0 HO TBDMSO TBDMSO HO HO, HO. (1] F G (2) H,O

Fill in the reagents below/above the arrow in the ff reaction