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- Predict the major product of the following reaction and draw it in the space provided. 1) NH,NH, 2) KOH, heatProvide the required information for the reaction scheme below: OH Compound B Compound C OH Compound A CHO CH2OH CHO CH2OH Compound E Compound D(R)-2-iodo-3-methylbutane is treated with sodium bromide in acetone. Select all products that are formed. 2-methylbutan-1-ol 2-methylbutan-2-ol 3-methylbut-1-ene (R)-3-methyl-2-butanol 2-methylbut-2-ene O (S)-2-bromo-3-methylbutane
- Draww all possible organic products and kinds of reactions (SN1, SN2, E1, E2)Determine the reagents required for the following syntheses. More than one reaction is likely required. a) b) c) d) OH OH olm NH₂ MeO NHMe Me. Me OH OHWhen cyclohexene is reacted with hydrobromic acid in acetic acid, the major product is bromocyclohexane. There is a small amount of cyclohexyl acetate formed. What is the mechanism that forms both compounds? What is the purification procedure that isolates both compounds?
- Draw the structural formula for the major product of the following reactions.Draw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism must account for all the products if more than one product is formed. 4-methycyclohexanol with phosphoric acid H3PO4 to for 1-methycyclohexene, 3- methylcyclohexene and 4-methycyclohexeneFill in the missing reactants, reagents, or products. More than one step may be needed to fill the boxes for missing reagents.
- Complete the reaction map by providing the answer from A-E. Write the IUPAC name of the products. conc HNO B conc H,SO, B, D FeBrs conc HNO, E AIC conc H2SO. conc H2SO4When trichloroacetaldehyde is dissolved in water, almost all of it is converted to the hydrate. Chloral hydrate, the product of the reaction, is a sedative that can be lethal. A cocktail laced with it is known—in detective novels, at least—as a “Mickey Finn.” Explain why an aqueous solution of trichloroacetaldehyde is almost all hydrate.a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity.

