Draw the structure for each of the following: a. phenyl acetate d. N-benzylethanamide e. y-methylcaproic acid f. B-bromobutyramide g. ethyl 2-chloropentanoate h. cyclohexanecarbonyl chloride i. a-chlorovaleric acid b. y-caprolactam c. sodium formate
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- (a) Give an acceptable name for compound A. (b) Draw the organic products formed when A is treated with each reagent: [1] H3O+; [2] −OH, H2O; [3] CH3CH2CH2MgBr (excess), then H2O; [4] LiAlH4, then H2O.Write out the steps needed to separate hydrocarbon A and carboxylicacid B by using an extraction procedure.Why is an alkylamine more basic than ammononia?
- Measure the weight of acetylsalicylic in aspirin. note: % of acetylsalicylic acid in aspirin is 5% provide a good expliationIzopropanole doesn't form by Select one: a. Hydration of propene b. Reduction of propanal c. Hydration of 2-chloropropane d. Reduction of propan-2-oneReaction with Strong Acids Table 9.8 Observations on the reaction of aniline with strong acids. Sample Observations +/- Aniline + H2SO4 Aniline + HCl Explain, in 1 – 3 sentences, the difference in the reaction of aniline with H2SO4 and HCl. ___________________________________________________________________________ ___________________________________________________________________________ ___________________________________________________________________________ Reactions: Aniline + H2SO4 Aniline + HCl
- Why some substituents make a benzene ring react faster than benzeneitself (activators) ?TRUE OR FALSE 15.In Fehling’s test, the theoretical product after an aldehyde is mixed with Fehling’s solution is alcohol. 16.Iodoform, which has a molecular formula of CH3I, is indicative that ketomethyl group is prresent. 17.Based on the physical property, hydroquinone has a lower boiling point compared to catechol. 18.When FeCl3 is used in visualizing aspirin in tin layer chromatography, the resulting spot is in red color.Tyramine is an alkaloid found in mistletoe and ripe cheese. Dopamine is a neurotransmitter involved in the regulation of the central nervous system. a. How can tyramine be prepared from β-phenylethylamine?b. How can dopamine be prepared from tyramine?c. Give two ways to prepare β-phenylethylamine from β-phenylethyl chloride.d. How can β-phenylethylamine be prepared from benzyl chloride?e. How can β-phenylethylamine be prepared from benzaldehyde?