1. 2-bromobutane + cyclohexanol + NaH à (major product)c. 2-butoxycyclohexanea.. 2-butenereactionb. 1-butened. noe. something else!2. t-butylbromide + sodium ethoxide in ethanol à (major product)a. 2-methylpropenereactionb. t-butyl ethyl etherc. 1-methylbutened. noe. something else!3. potassium t-butoxide + 1-bromobutane in t-butyl alcohol roomtemperature à (major product)a. 1-butenereactionc. 2-methylpropene d. nob. butyl t-butyl ethere. something else!4. t-butyl bromide + boiling hot water à (major product)a. 2-methylpropenereactionb. t-butyl ethyl etherc. t-butanold. noe. something else!5. 2-chloropropane + acetic acid (2 eq) / KOH (1 eq) / DMF à(majorproduct)c.b.d. no reactione. somethingа.HO.else!BrKOH / DMSO6.b. 2-methyl-1-propanold. 1,2-a. 2-methylpropenepropanedienec. no reactione. something else!7. cyclopentanol+ NaH + DMSO + bromopropane à(major product)a. cyclopentenereactionb. propenee. something else!!c. propyl cyclopentyl etherd. no8. 2-bromo-3-methylbutane + KOH / DMSO à(major product)a. 2-methyl-1-butened. no reactionb. 2-methyl-2-butene c. 3-methyl-2-butanole. something else!!9. 2-chloro-3-methylbutane + KI/ DMSO à(major product)a. 2-methyl-1-butened. no rxnb. 2-methyl-2-butenec. 3-methyl-2-iodobutanee. something else!!10. (S)-2-iodobutane + NaN3 / DMF à (major product)a. Vb.d. Ve. no rxnf. something else!!11. cyclohexene + NBS/ CCI, / light followed by K* t-butoxide / t-butanolwith heating àa. cyclohexene b. 1,3-cyclohexadienecyclohexane e. something else!c. 1,2-cyclohexadiene d.

Answered: Image /qna-images/answer/a0dd186a-674c-47ae-8a75-979d7f9e9b6b.jpg

1. 2-bromobutane + cyclohexanol + NaH à (major product) c. 2-butoxycyclohexane a.. 2-butene b. 1-butene d. no reaction e. something else! 2. t-butylbromide + sodium ethoxide in ethanol à (major product) a. 2-methylpropene reaction e. something else! b. t-butyl ethyl ether c. 1-methylbutene d. no 3. potassium t-butoxide + 1-bromobutane in t-butyl alcohol room temperature à (major product) a. 1-butene b. butyl t-butyl ether c. 2-methylpropene d. no reaction e. something else! 4. t-butyl bromide + boiling hot water à (major product) a. 2-methylpropene reaction e. something else! b. t-butyl ethyl ether c. t-butanol d. no 5. 2-chloropropane + acetic acid (2 eq) / KOH (1 eq) / DMF à(major product) c. а. b. с. d. no reaction e. something else! Br KOH / DMSO

1. 2-bromobutane + cyclohexanol + NaH à (major product) c. 2-butoxycyclohexane a.. 2-butene b. 1-butene d. no reaction e. something else! 2. t-butylbromide + sodium ethoxide in ethanol à (major product) a. 2-methylpropene reaction e. something else! b. t-butyl ethyl ether c. 1-methylbutene d. no 3. potassium t-butoxide + 1-bromobutane in t-butyl alcohol room temperature à (major product) a. 1-butene b. butyl t-butyl ether c. 2-methylpropene d. no reaction e. something else! 4. t-butyl bromide + boiling hot water à (major product) a. 2-methylpropene reaction e. something else! b. t-butyl ethyl ether c. t-butanol d. no 5. 2-chloropropane + acetic acid (2 eq) / KOH (1 eq) / DMF à(major product) c. а. b. с. d. no reaction e. something else! Br KOH / DMSO

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Give 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-dimethylnonane
Show how to convert propene to each of these compounds, using any inorganic reagents as necessary. a. Propane b.1,2-Propanediol c. 1-Propanol d. 2-Propanol e. Propanal f. Propanone g. Propanoic acid h. l-Bromo-2-propanol i. 3-Chloropropene j. 1,2,3-Trichloropropane k. 1-Chloropropane l. 2-Chloropropane m. 2-Propen-1-ol n. Propenal
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2 mehgiheene ..syclohexene. HO H. P-benzoicacid.
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