Identify the hydrolysis product of the cyclic enamine below 1) H30* 2) NaOH Ph The compound below Ph The compound below Ph The compound below Ph The compound below Ph
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- Which of the following reactions represents the most likely reaction of naproxen with water? a.) C14H14O3(aq) + H2O(l) ⇄C14H13O3-(aq) + OH-(aq) b.) C14H14O3(aq) + H2O(l) ⇄C14H15O3+(aq) + OH-(aq) c.) C14H14O3(aq) + H2O(l) ⇄ C14H13O3-(aq) + H3O+(aq) d.) C14H14O3(aq) + H2O(l) ⇄C14H15O3+(aq) + H3O+(aq)Rank the following compounds in order of increasing basicity: I. p-nitroaniline III. N-methylaniline II. p-aminobenzaldehyde IV. p-methylaniline17.36 Tamoxifen is an estrogen receptor modulator that is used in the treatment of breast cancer. Provide the missing reagents and the structure of compound A in the synthesis of tamoxifen. Page 707 HO (CH3)2N 1. C,H,MgBr 2. H + Compound A (CH3)2N Tamoxifen
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- Ester group (e.g. -CO2Et) is considered a .... Ortho/Para Directing Activator Ortho/Para Directing Deactivator Meta Directing DeactivatorDraw the mechanisms for the reactions between the given carboxylic acid and LDA in THF at -78 deg C.Identify the lettered compounds in each reaction sequence.Draw the product formed when phenylacetonitrile (C6H5CH2CN) istreated with below reagent. [1] DIBAL-H; [2] H2O
- Reduction of an alkyl azide results in the formation of —-. A. an imine B. an oxime C. a tertiary amine D. a secondary amine E. a primary amine2 Draw structures to correspond with the following common and systematic names:(a) phenyl formate (b) cyclohexyl benzoate (c) cyclopentyl phenylacetate(d) N-butylacetamide (e) N,N-dimethylformamide (f) benzoic propionic anhydride(g) benzamide (h) g-hydroxyvaleronitrile (i) a-bromobutyryl chloride(j) b@butyrolactone (k) phenyl isocyanate (l) cyclobutyl ethyl carbonate(m) d@caprolactam (n) trichloroacetic anhydride (o) ethyl N-methyl carbamateShow how you would convert propan-1-ol to the following compounds using tosylateintermediates. You may use whatever additional reagents are needed. b) propan-1-amine, CH3CH2CH2NH2