Please name the two diene products that could be obtained in the double-dehydration reaction of hexane-2,4-diol, and next identify the major product
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Please name the two diene products that could be obtained in the double-dehydration reaction of hexane-2,4-
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- Name the two diene products that could be obtained in the double-dehydration reaction of hexane-2,4-diol, and identify the major product. Please explain in words rather then imagesname the two diene products that could be obtained in the double-dehydration reaction of hexane-2,4-diol, and identify the major product.Please provide the name of the dienes and dienophiles, and their products and explain the reaction that took place in each item.
- The Wittig reaction can be used for the synthesis of conjugated dienes as the example below, 1-phenyl-penta-1, 3-diene. Propose two different sets of reagents that could be combined in a Wittig reaction to give 1-phenyl-1,3-pentadiene.The 3D image below is that of an allylic carbocation intermediate formed by the protonation of a conjugated diene with HBr. Draw structural formulas for the final reaction products.1. Write the complete thermal reaction to get the product below. Include reagents and conditions. Write brief explanation about the reaction mechanism. 2. Write the thermal reaction of the compound below with buta-1,3-diene. Write reagents and conditions. Write brief expanation about the reaction mechanism.
- find the carboxylic acid that can be prepared from 4-bromomethylbenzenea. by direct oxidationb. by free radical chlorination followed by nitrile synthesisDetermine all of the products obtained from the addition of HCl to the 1,3-diene. Once determined, draw a mechanism that accounts for the formation of every product. Then, Identify and account for the formation of the major adduct/or adducts under these conditions assuming that the reaction is conducted under thermodynamic conditions.Show the process of synthesizing 2-methyl2-cyclohexenone from 2-methyl cyclohexanone. Write down the stages of the monocyclic reaction process in detail.
- Addition of HBr to 3,3-dimethyl-1-butene gives a mixture of two isomeric alkyl bromide products. Please daw structures for the two products, and give a mechanistic explanation for their formation.Predict the structure of the product formed when HCl adds to 1-Bromo cyclohexene. Also explain how this prediction is in accord with ortho, para-directing effect of bromine on an aromatic ring?Explain and show hydroboration-oxidation mechanism of trans-1,3-dimethylcyclohexane.