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- Determine the major product of the following reaction H3O*Predict the products of the following reactions. ethoxybenzene + concd. HI, heatWhat explains why many aldehydes and ketones can undergo self- condensation reactions in basic conditions? The alpha carbon can lose a proton and act like a nucleophile and the carbonyl carbon a an electrophile O The alpha carbon can gain a proton and act like an electrophile and the carbonyl carbon is a nucleophile O The oxygen of the carbonyl group can attack the carbon of the carbonyl group Only esters can undergo self-condensation reactions
- CCH H20, H2SO4 H9SO4 CH3 Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presence of mercury(II) sulfate as a Lewis acid catalyst. The reaction occurs with Markovnikov regiochemistry, so the OH group adds to the more highly substituted carbon and the H adds to the less highly substituted carbon. The initial product of the reaction is a vinyl alcohol, also called an enol. The enol immediately rearranges to a more stable ketone via tautomerization. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Hjö: -CH3 -CH3 H3O*Predict the b-elimination product(s) formed when each bromoalkane is treated with sodium ethoxide in ethanol. If two or more products might be formed, predict which is the major productDraw the major organic product of the following reaction: Br₂ HO,
- In the presence of heat or light, diazomethane is converted into a carbene that adds to alkenes. Draw the correct products for the following reaction.Draw the products (including stereoisomers) formed when 2- methylhex-2-ene is treated with HBr in the presence of peroxides.When carbonyl compounds are reduced with a reagent such as LiAlH4 or NaBH4 and a new stereogenic center is formed, what will the composition of the product mixture be? Forms more of one enantiomer than another because of steric reasons around the carbonyl Forms more of one enantiomer than another depending on the temperature of the reaction Forms different products depending on the solvent used Forms a racemic mixture of the two possible enantiomers
- Which of the following is a primary alkyl halide? O cyclohexyl bromide O isopropyl bromide Ot-butyl iodide O isobutyl chloride Omethyl bromideDraw the alkene reactant of the following reaction. n 6 H3o+ H3C OH H20What is the product of the following reaction? H₂, Pt cyclohexanol cyclohexane cyclohexene 1,2-cyclohexanediol