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Perform a retrosynthetic analysis and draw the starting material
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- Draw the products for the following substitution reactions:Propose a synthesis of the topical anesthetic cyclomethycaine from 4-hydroxybenzoic acid, 2-methylpiperidine, and any other necessary reagents. HN' + HO. НО Cyclomethycaine 4-Hydroxybenzoic acid 2-MethylpiperidineWhat products are formed when the amine below reacts with HC1? CH,CH,CH,-N- -N-CH,CH,CH-CH,CH;CH, A) CH;CH,CH, NH, + CH,CICH,CH;CH;CH;CH, B) CH,CH,CH,- CH,CH CH,CH,CH,CH, + CI C) CH,CH,CH,-N-CH,CH-CH-CH,CH,CH, H,CI D) CH,CH,CH, N-CH,CH,CH,CHCH,CH, + CI"
- A mixture of the compounds shown below is dissolved in cyclohexane. An aqueous solution of NaOH is added to the solution, and two layers are formed. Which compound(s) is(are) found in the aqueous layer? он HO Benzoic acid Beta-naphthol Naphthalene O Benzoic acid only O Beta-naphthol only O Naphthalene O Both Benzoic acid and beta-naphthol O Both beta-naphthol and naphthaleneThe compound below can form a hemiacetal by reacting with itself in solution. What is the structure of this hemiacetal? HO H. о но H о но Н НО ОН ОН ОНAmong the choices shown, which reagents would lead to 3-pentanone from bromoethane? Al 1 Li Cul 2) C13CH2OTS | BI1 NECNn DMSO 2) CH3CH2M;Br 3)H2O C)CH13CH2-CO CI D CH3CH2-CO OCH2CI13
- Rank the reactivity of the compounds below toward nucleophilic acyl substitution by writing the compounds' letters in the proper blanks in the box below. `NH CI Br CH3 CH3 A В C E rank compounds for acyl substitution reactivity most least reactive reactiveThe following compound forms a six-membered cyclic hemiacetal. Select the -OH group (A, B, C, D) that takes part in this reaction. сно H- OH H- (он) А в но -H C HO H- CHOH D Select one: O A ов O CYou identified aldehydes or ketones by converting them into hydrazones. Which of the following molecules contains a hydrazone functional group? O2N A) B) O,N -NO2 HN- -NO2 C) O,N D) O2N HN- -NO2 NO2 NH OC
