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In the acid-catalyzed aromatic alkylation involving 1-methylcyclohexene and benzene, two isomeric products are possible, but only one is formed, as shown here. Draw the complete mechanism that leads to each product, and explain why only one isomer is formed.

Question: Draw the mechanism of the reaction you will complete in lab. Use the proper arrow drawingconvention to show all bond making and bond breaking steps in the reaction.   Background info: A substitution reaction takes place when a nucleophile (Nu:) forms a bond with a carbonatom, displacing a leaving group (L).SN2 reactionLeaving groups are typically weak Bronsted bases that are stable as anions (often halide anions).The precise timing of when the leaving group leaves depends on the structure of the substrate –the molecule bearing the leaving group. Methyl and primary alkyl halides tend to undergo SN2type reactions. In this type of reaction, the nucleophile attacks the carbon from the side oppositethe leaving group and the nucleophile-carbon bond is made simultaneous with the carbon-leavinggroup bond breaking. SN2 reactions are one-step and there is an inversion of stereochemistry atthe carbon bonded to the nucleophile.SN1 reactionIf the carbon undergoing substitution is…

Draw the major product of this reaction. Include stereochemistry if applicable. Ignore byproducts. CH₂OH heat

Identify the major organic product of this reaction and draw the mechanism.

Draw the complete, detailed mechanism (curved arrows) for the following reaction. Br 2. H₂O OK

For this problem, draw all hydrogen atoms explicitly. Part A Draw the product of the hydrogenation of ethyne.

This reaction is incorrect as written. In the box below draw the structure of the correct product.

Predict the major product of the reaction.