Ses) 184875/quizzes/secured#lockdown 问题10 59 Although the yields might be low, what are the reasonable starting materials to achieve this compound? HCI A. benzylic acid and 1,5-pentanediol B. cyclohexanone and 1,4-butanediol C. cyclohexanone and 1,3-propanediol D. 1,2-cyclohexanedione and propanol E. cyclohexanecarboxylic acid and propanol O A

Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. Br Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H₂SO4 c. HCI d. HBr e. SOCI₂ g. CrO3, H₂ SO4, H₂O h. NaH Reagents available i. CH3 MgBr; then H3O+ j. CH3 CH₂ MgBr; then H3O+ k. CH3 CH₂ CH₂MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP) Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3

IUPAC naming and alcohol reactions

The major product of the reaction below is OH H* heat A. 3-methyl-1-butene B. 2-methyl-3-butene C. 3-methyl-2-butene D. 2-methyl-2-butene

H H-C-OTC -C- C-CH n HOMEWORK 1. Write a structural formula for each of the following: a. An alcohol C3H80 b. An ether C4H100 c. An aldehyde C3H60 d. A ketone C3H60 e. A carboxylic acid C3H6O2 f. An ester CsH 10O2 2. Write an equation for the reaction of CH2=CHCH2CH3 with each of the following reagents: a. Hydrogen chloride b. Hydrogen (Pt catalyst) c. Ozone, followed by Zn, H* d. BH3 followed by H2O2, OH e. Bromine f. H2О, H* g. KMnO4, OH h. Oxygen (Combustion)

Q1. Name parts a through d - draw parts e through h: CH3-CH2-CH-CH,-NH, ČH3 a. b. CH3 'N' H3CH2C ČH3 с. NH2 Br d. e. 2-chloropentan-2,3-diamine f. N-ethyloctanamide g. N-ethyl-N-methylbutanamide h. 3-methylbutan-1-amine

34. Which compound has the highest oxidation state? A) CO₂ B) CH4 C) CH₂OH D) CH2Cl₂ 35. Which alcohol below can be prepared using MeMgBr as a nucleophile with an aldehyde electrophile? A) 2-methyl-1-butanol B) 2-propanol C) 3-hydroxy-3-ethylpentane D) 1-propanol 36. Which reagent would be the greenest and best reagent for epoxidation of propylene A) B) C) D) CHCOH Cl₂ and H₂O followed by NaOH Oxygen and a catalyst Ozone