Predict the product of the following reaction and name the product H₂C CH3 OH conc. H₂SO4 Explain the mechanism by which this reaction proceeds
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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.Reaction of but-1-ene with HBr gives two products in unequal amounts. In each case, identify the two products, state which is the major product, explain why it is the major product and give the mechanism for its formation.When 2-methylpent-2-eno reacts with HCl two alkyl halides are formed. Present the structures of the formed products and propose a mechanism that explains the formation of these products. Indicate the main product.
- Write a mechanism that accounts for the formation of ethyl isopropyl ether as one of the products in the following reaction. CI OEt HCI EtOH Write the mechanism for step one of this reaction. Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. Write the mechanism for step two of this reaction (where the product of step one reacts with the solvent, ethanol). Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. Write the mechanism for the last step of this reaction (formation of ethyl isopropyl ether). Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. CI will act as the base in this reaction.Compound A reacts with the reagents shown in the image. Write the mechanism, step by step, for the formation of product B. Note that B has the molecular formula C14 H18 O.Predict the product of the following reaction. A OH HNO3, H2SO4 B Name the organic product without stereochemistry. What is the molecular formula of the product?
- When propene reacts with gaseous hydrogen bromide, HBr, two products, 1-bromopropane and 2-bromopropane are formed. The reaction is a two-step process in which the electrophilic attack occurs in the first step. Identify the electrophile in this reaction Draw a diagram showing the first step of the reaction that leads to the production of 2-bromopropane.provide the hydrotreating for the organic compoud C9H7N in a more detailed way? regarding which bond will break first and how many steps the reactant will go through to reach the product shown.4eplease give the resulting product and explain
- CoO7T07Q3769 Give the major product of the following reaction. H2 Ni CIPredict the product. Draw the structure(s) of the major organic product(s) formed in the following reactions. Please indicate stereochemistry if appropriate.By taking into account electronegativity differences, draw the products formed by heterolysis of the carbon–heteroatom bond in each molecule. Classify the organic reactive intermediate as a carbocation or a carbanion.