Complete these nucleophilic substitution reactions . In each reaction, show all electron pairs on both the nucleophile and the leaving group (a) Br+ CH₂O¯Na+. methanol (b) Cl + NH3 ethanol
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- 4) Rank the following compounds in order of increasing reactivity (least to most reactive) with respect to acyl substitution. I. methyl benzoate II. benzoylchloride III. benzamide III < | < ||12) Use the curved arrow formalism to show the movement of electron pairs in the following reaction and label each reactant as a nucleophile or an electrophile. CHÍNH CHỊCH, + CO Học Nha CH₂CH₂CIPQ-2. This reaction is classified as (A) a nucleophilic addition. (C) a nucleophilic substitution. NaCN H3C CH3 H₂O (B) an electrophilic addition. (D) an electrophilic substitution. HO H3C CN CH3
- a) b) - Fill in the reagents above/below the arrow in the following reactions. c) CN F CO₂H OH ХонDraw the structure(s) for the major final product(s) formed in the following reaction sequence. CN ༼་་ SO 503 H₂SO4 Cl FeCl3 Click and drag to start drawing a structure.A synthetic organic molecule, G, which contains both aldehyde and ether functional groups, is subjected to a series of reactions in a multi-step synthesis pathway. In the first step, G undergoes a Wittig reaction, leading to the formation of an alkene, H. Subsequently, H is treated with an ozone (O3) reagent followed by a reducing agent in an ozonolysis reaction, resulting in the formation of two different products, I and J. Considering the functional groups present in G and the nature of the reactions involved, what are the most probable structures or functional groups present in products I and J? A. I contains a carboxylic acid group, and J contains an aldehyde group. B. I contains a ketone group, and J contains an alcohol group. C. I and J both contain aldehyde groups. D. I contains an ester group, and J contains a ketone group. Don't use chat gpt.
- 4) Give an example of an enol which would tautomerize into a) an aldehyde and b) a ketone.Draw a Lewis structure of sodium ethyl mercaptide (NaSC2H5), showing all relevant lone pairs and formal charges. Based on the structure you drew, do you expect that it would act as a good nucleophile? Do you expect it to act as a strong base?The SN2 reaction is an example of a nucleophilic substitution reaction. Draw the structure of the two reactants and the mechanism of the reaction. The reaction is 1-bromo-3-ethylpentane reacts with cyclohexanol under basic conditions.
- Draw the structure of the starting material needed to make 2-methylhept-3-yne using sodium amide in liquid ammonia, followed by 1-bromopropane. The starting hydrocarbon must have no more than five carbons 1) NaNH2, NH3() NaBr + 2) CHзCH2CH2BrDraw the structural formula for the major product of the following reactions.Complete the following nucleophilic substitution reactions. In each reaction, show all electron pairs on both the nucleophile and the leaving group.
