Which of the reactions shown would produce isopropylbenzene as the major product? OIV all of these O III 1 CI = AICI 3 H₂SO4 H₂SO4 11 OH IV AICI 3
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- Provide the mechanism for the conversion shown below. CH3Li is effectively H3C-Li+. What type of mechanism is occuring?From letters, C to G predict the products for the following reactions. Indicate NR if there is NO REACTION.Are there any other possible products for the following reaction in catalytic H2SO4 and H2O?
- Given below is the reagent of a reaction. Predict the products of the following reactions: Indicate NR if there is no reaction.Explain the mechanism-Carboxylation—Reaction of RMgX with CO2Under forcing conditions, sp2 CH bonds can be deprotonated, and sp2 chlorides can be eliminated. Draw two different mechanisms to account for the formation of the isomeric products C3H4 from the same chloride starting material.
- Draw the mechanism fot his reaction. B = [IrCl(CO)(PPH3)2]In light of your answer to Problem 30-40, explain why a mixture of products occurs in the following reaction:All attempts to isolate primary and secondary nitroso compounds result solely in the formation of oximes. Tertiary nitroso compounds, however, are stable. Explain.
- What products are formed when the following molecule reacts with catalytic H2SO4, H2O, and heat? Please show the mechanism for the reaction.M 6 write the principal product in a, c & e and the neccesary reactives for b, d & f in the following reactions :Please predict the product of the given reactant to complete the reaction. Indicate NR if there is no reaction.