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Q: Please provide synthesis showing reagent steps to get to the product compound. I appreciate your…
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Please provide synthesis showing reagent steps to get to the product compound. I appreciate your help.
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- 5.Synthesis. Make the following products from a suitable cyclic alkene starting material. Look at the functional group PATTERN present in the molecule, including stereochemistry. Br CH 3 Br CH3Oxidize the below molecule as many times as possible. Then name each product. ОН CH3 `CH3 H3C. ...Which structure is most correct for (2E)-but-2-en-1,4-diol? OH HO OH H,C. CH, HO. H,C HO OH HO
- 1. Draw structure of the products of the reactions KMN04 ? Acetone NaOH H ELOH H. КОН ? Ethanol 2.3. Please draw the most important (stable) resonance form of the carbonation that mediates the following reaction: OH H3O+ O 4. Draw the structure of the alkene isomer (with the molecular formula of C5H10) that is most reactive one in the addition reaction with Br₂.a. The following compounds have the same molecular formula as benzene. How many monobrominated products could each form? 1. HC‚CC‚CCH2CH3 2. CH2“CHC‚CCH“CH2 b. How many dibrominated products could each of the preceding compounds form? (Do not include stereoisomers.) c. How many dibrominated products could each of the compounds form if stereoisomers are included?
- 36. Which of the following is a tertiary alkyl halide? A. (CH) CHBr B. (CH) CHCH.C C. (CHICCI D. CH.CHICHI E. CH.CHB 37. What is the product? CM₂ CH₂CH-CH(CH₂CH₂OH CH, A H,CH₂CCHICH OCH₂ AA B.B C.C substitution only CH₂ B (H₂CMC-CHICH, OCH C. both A and B1. Reaction of 2,3-dimethyl-1-butene with HBr leads to an alkyl bromide, C6H13Br. On treatment of this alkyl halide with KOH in methanol, elimination of HBr occurs and a hydrocarbon that is isometric with the starting alkene is formed. What is the structure of this hydrocarbon and how do you think it is formed from an alkyl bromide? 2. 1-Octen-3-ol is a potent mosquito attractant commonly used in mosquito traps. A number of reactions, including hydrogenation, will transform 1-Octen-3-ol into a less effective molecule. Write a complete reaction equation for the hydrogenation of this alkenol.9. Which of the following alkenes has a Z configuration?
- 5. Give the IUPAC name of the following carboxylic compounds. а. CH,СH,С-ССООН b. CH,CH(NH;)CH(OH)COOH c. (CH;)C=CHCOOH d. CH3 СООН е. NO, .COOH O,N `NO, 6. Draw the structure of the following compounds. a. cyclobutanecarboxylic acid b. 3,3-dimethylpentanedioic acid c. 4-aminopentanoic acid d. 2-methylcyclohexanecarboxylic acid e. m-chlorobenzoic acidGive the structure corresponding to each name.a. 3-chloro-2-methylhexaneb. 4-ethyl-5-iodo-2,2-dimethyloctanec. cis-1,3-dichlorocyclopentaned. 1,1,3-tribromocyclohexanee. sec-butyl bromidef. 6-ethyl-3-iodo-3,5-dimethylnonane2. Name each alkyne. a. CH3CH₂CH₂C=CH b. CH3CH₂CH₂C=CCH3 3. Predict the product of the following reactions. a. CH = CCH3 + HCI b. CH CCH₂CH3 + O2