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- based on this video: on Hinsberg Test Tests for Amines - MeitY OLabs (8.5min) https://www.youtube.com/watch?v=j5jgMUWri8U Write the reaction (two-step, in skeletal) of each test amine when tested in the Hinsberg Test.Which of the following compounds is likely the least reactive in dilute aqueous NaOH? A. EtCOCl B. CH3CONEt2 C. CH3C(O)OC(O)CH3 D. CH3COOEtArrange the following compounds in order of decreasing acidity.CH3COOH CH3OH CH3CH3 CH3SO3H CH3NH2 CH3SH CH3C‚CH
- All of the following compounds can react as acids. Without using a table of acidities, rank them in order of increasing acidity. Explain your ranking.(a) CH3CH2SO3H (b) CH3CH2OH (c) CH3CH2COOH(d) CH3CHClCOOH (e) ClCH2CH2COOHRank the compounds below in order of increasing acidity HF, H2O, NH3H3C-O-SiH3 ether, which is similar to dimethyleters, was synthesized. This ether is known to be a weaker base than (CH3)3O. Discuss why and explain
- i) 3-methyloctane-2,3-diol 11) 3-chloro-4-ethoxy-2-methylcyclopentanamine iii) N, N, 3,3-tetramethylbutan-2-amine iv) 1-ethoxy-2,5-difluorohexan-3-ol 6) 5-isopropoxy-3-isopropyl-6-propoxy-4-propylcyclohexane -1, 2-diol draw of the following names in skeletal forms__________ will exist as a racemic mix. Chloro ethyl methyl amine Phenyl amine Ammonia Methyl diphenyl propyl ammonium chloride Diethyl amine Thank you!Rank the following compounds in terms of increasing acidity:I. C2H5OHII. C6H5OHIII. NaOC2H5IV. CH3COOH
- 2-cyanophenol (pka 7.0) is even more acidic than the 4-cyanophenol isomer. Propose an explanation of why it is so.Starting with benzene, what is a possible product of this series of reactions?: 1) HNO3 & H2SO4 2) Fe, HCl 3) (CH3)2CH-Br, FeBr3 4) NaNO2, HCl, 0-10 oC 5) HBF4 2-fluoro-3-isopropylaniline m-fluoro-benzenesulfonic acid o-fluoro-isopropylbenzene 2-amino-benzenesulfonic acidselect the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4