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- Write a mechanism for the reaction below. Hint: think retro!Using only organic reagents of 4 carbons or fewer, as well as any necessary solvents/inorganic reagents, propose a synthesis of the molecule below. Assume all products can be separated easily. If more than one product is to be expected in any step, indicate which product will be taken further.Elaborate an efficient synthesis of the molecule below starting from benzene (your choice). Mechanisms are not required
- Outline a multi-step synthesis of the compound shown below starting from benzene.Propose a synthesis of the compound below using only ethyne, methyl bromide, and methanol as sources of carbon. Is the product optically active? ExplainAfter E2 elimination, will this product contain deuterium (D)? Justify your answer.
- Propose a detailed mechanism for the reaction below (in the attached picture), showing the structure of thestable intermediate and using curved arrows to indicate electron flow in each stepshobha Propose a plausible mechanism for each of the reactions below with clear arrow pushingwrite out a complete mechanism for the reaction below