Q: Chemistry
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- 17-45 How would you synthesize the following alcohols, starting with benzene and other alcohols of six or fewer carbons as your only organic reagents? (a) (b) (c) OH CH₂CH3 HO CH3 CH₂CH₂CH3 CH3 CH3CH₂CH₂CHCH₂CH₂OH (d) CH3 OH CH3CHCH₂CHCH₂CH3Draw the structure of the following compounds which parent names have been traced to a common name; (a)5-methyl-4-nitroimidazole (b)2-chloro-4-methoxythiazole.17-48 How would you prepare the following compounds from More than one step may be required. 1-phenylethanol? (a) Acetophenone (PhCOCH3) (b) Benzyl alcohol (c) m-Bromobenzoic acid (d) 2-Phenyl-2-propanol 17-49 How would you prepare the following substances from cyclopentanol? More than one step may be required. (a) Cyclopentanone (b) Cyclopentene (c) 1-Methylcyclopentanol (d) trans-2-Methylcyclopentanol 17-50 What products would you expect to obtain from reaction of 1-methyl- cyclohexanol with the following reagents? (a) HBr (b) NaH (c) H₂SO4 (d) Na₂Cr₂O7
- Draw the line structures and provide common names for the following ketones: (a) 1-Phenylpropanone (b) 2-Methylpentan-3-one(c) 1-Cyclohexyl-3,3-dimethylbutan-2-one14. What is the IUPAC name for the following compound? NH- (a) propyl propanamide (b) propyl propanoate (c) N-propylptopanamine. (d) N, N-propylpropanamide (e) N-propxlpropanamideWhich of the following would successfully perform the shown reaction? (A) (B) (C) (D) OH 1) NaH 2) EtBr NEt3 Mgº ether MeO OMe [TSOH] H ? PCC
- Write the products of the following acid-base reactions: (a) CH3OH + H2SO4 ² ? (b) CH3OH + NANH2 2 ? (c) CH3NH3+ Cl- + NaOH ?11) Synthesize 2-methyl-3-hydroxycyclohexone from cyclohexone, methyl iodide, and inorganic precursors.Draw structural formulas for these ketones. (a) Ethyl isopropyl ketone (b) 2-Chlorocyclohexanone (c) 2,4-Dimethyl-3-pentanone (d) Diisopropyl ketone (e) Acetone (f) 2,5-Dimethylcyclohexanone