Please give a detailed stepwise mechanism for the following reactions. All arrows, charges, and intermediates must be shown. 1) CN H*, H₂O, heat Яон OH
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- Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes) rearrangement. Keeping this in mind, draw a stepwise mechanism that forms all of the following products.Identify the major product of the following reaction sequence. 1) [H*], H₂NNH2, (-H₂O) 2) KOH/H₂O, heat HO₂C HO₂C HO CO,H OH OH There is no reaction under these conditions or the correct product is not listed here.
- 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-methycyclohexeneProvide the major products of the given reaction.NH 1) xs Mel 2) Ag2O, H2O, A 2. Complete the following reaction. Show the intermediate, and propose a mechanism for the second step.
- Give the major organic product of the following reaction. 1) ВНз 2) H202, NaOH HO- OH HO There is no reaction under these conditions or the correct product is not listed here.pls also name the major product, thanks!Give the major product of the following reaction. 1) OsO4 ? 2) NaHSO3, H2O Ph, он "ph H' Но Ph H OH Но Ph H' Ph Ph Ph Ph Ph Ph C There is no reaction under these conditions or the correct product is not listed here.
- Provide a mechanism for the following reaction. Show each step in your mechanism and use curved arrows to show the movement of electron pairs. Hint: the first step is a proton transfer; second step, nucleophilic attackGive the major product of the following reaction. 1) ВН3/THF 2) H202, NaOHAlkyl diazonium salts are unstable even at low temperature. They decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes) rearrangement. Keeping this in mind, draw a stepwise mechanism that forms all of the following products. NANO2 он + HCI, H2O NH2 он