Reaction of excess Grignard reagent with the following compound gives a(n) as the final product (following acidic workup). CH3CH2- O CH2CH3 a.) Ketone c.) Secondary alcohol b.) Ester d.) Tertiary alcohol
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- The reaction of H with tert-butyl ethyl ether would producea.) tert-butyl iodideb.) tert-butyl alcoholc.) z-methvloropene d.) iodoethaneIUPAC name of the structures4. Provide an alternative method for the preparation of cyclohexene from another compound than cyclohexanol. Give a reaction equation only D, Focus nited States) oto acer
- please answer d, e, f1. The acid-catalyzed elimination of an alcohol is an equilibrium reaction and requires special reac- tion conditions to favour the formation of the alkene product. What chemical principle controls the amount of alkene product that is produced? Provide two laboratory techniques that can be used to obtain good alkene yields in alcohol elimination reactions.Which reagent could be used to prepare propanoic acid from propan-1-ol?a.) periodaneb.) mCPBAc.) CrO3/H2SOAd.) Cl2
- 2) Synthesize each compound from the given starting materials using the Suzuki reaction CH3CH₂CH₂-C=C-H a. b. C. CH3O CH₂O Br +Starting with cyclohexanone, show how to prepare these compounds. In addition to the given starting material, use any other organic or inorganic reagents as necessary. a. Cyclohexanol b. Cyclohexene c. cis-1,2-Cyclohexanediol d. 1-Methylcyclohexanol e. 1-Methylcyclohexene f. 1-Phenylcyclohexanol g. 1-Phenylcyclohexene h. Cyclohexene oxide i. trans-1,2-CyclohexanediolReagents a. C6H5CHO b. NaOH, ethanol h. BrCH2CH=CH2 i. Na* OEt, ethanol j. Br2, H* k. K* t-BuO c. Pyrrolidine, cat. H* d. H2C=CHCN e. H3O* f. I. CH2(CO2ET)2 -CH2CH2CN LDA m. heat g. ELOC(=0)CO2ET Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda).
- Identify the organic functional groups and reaction type for the following reaction if only the major product is shown.The reactant is a(n) :a. phenolb. secondary alcoholc. tertiary alcohold. primary alcohole. alkeneThe product is a(n)a. alkeneb. carboxylic acidc. aromaticd. alkynee. aldehydef. etherThe reaction type is :a. hyrolysisb. reduction (hydrogenation)c. oxidationd. hydratione. dehydration2. Functional Groups Name each nitrogen-containing functional group in the following molecule a = a b = H3C CH3 C = Provide a generic structure (e.g. R = alkyl group) for the following functional groups d. epoxide e. peroxide(a) 2-methyl-2-pentanol Draw the structure of the alkene that was used to prepare the alcohol in highest yield. 8 ? ChemDoodleⓇ Which process does this employ? 1. Hg(OAc)2, H₂O; 2. NaBH4 1. BH3; 2. H₂O2, NaOH OsO4, H₂O2 #[ ] در On