Show how you would synthesize the following compound using 4-methylhex-1-ene starting material and any reactions we have talked about in this course. OH OH
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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.Show how you would synthesize the following compounds from alkyl halides, vinylhalides, and aryl halides containing no more than six carbon atoms. trans-oct-3-eneShow how you would synthesize the following compounds, starting with acetylene and any compounds containing nomore than four carbon atoms. pentanal, CH3CH2CH2CH2CHO
- Provide reagents/conditions to accomplish the following syntheses. Several steps are required in some cases. H2N NH2 Но TH. NH2 HOStarting from bromobenzene and any other reagents and solvents you need, show how you would synthesize the followingcompounds. Any of these products may be used as starting materials in subsequent parts of this problem. 2-phenylbut-2-ene1. Provide stepwise synthesis including reagents and intermediates for the following syntheses. OH COOH
- Select the reagents that will allow the following transformation(s) to occur. -H ? 1) NaOH 2) propyl bromide 1) Na2HSO4 2) propylanol 1) NaOH 2) propyl bromide 1) NaNH₂ 2) propyl bromideOchem IUPAC names Can you please see if I have named these correctly (see the attached image for the compound structures) I have them named as follows: 1-iodo-4-methoxy-2-nitrobenzene 3-bromo-5-phenylaniline 4-cyclopentyl-2-hydroxybenzoic acid 3-methyl-1-phenylbutan-1-ol If these are incorrect please correct them!Starting with benzene and using any other necessary reagents of your choice, what are the possible syntheses for the following compound?
- Show how to synthesize the following product as the major product starting with 2,2-dimethylpropane as the starting material. You may use additional reagents and any number of steps. Be sure to list each step with all reactants/reagents/conditions required. (Do not use hydrogenation reactions). Write the process.Synthesize the compound below from benzene. COOH NO₂Show how you might prepare each compound by a Heck reaction using methyl 2-propenoate as the starting alkene.