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- Draw the favored product(s) of the following reactions (organic chemistry)What products are formed when each of the following reacts with HO-? a. CH3OH b. +NH4 c. CH3N+H3 d. BF3 e. +CH3 g. AlCl3 d. BF3 f. FeBr3 h. CH3COOHThese reagents can produce ketones with alkynes A. BH3, THF, H2O2 B. KMnO4 C. O3 D. H2SO4, H2O, HgSO4 choices:A,DB,CA,B,CA,B,C,D
- Which of the following compounds reacts most rapidly in a nitration reaction?Which of the following compounds shows the strongest acidity A-ch3oh B-ch3ch2oh C-h2o D-c6h5oh E-ch3och3Arrange the following carboxylic acid derivatives in their correct order of reactivity. 1=Most reactive and 4=least reactive.
- Choose the most correct set of reagents for the following reaction.Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict themajor products of the reactions of naphthalene with the following reagents.(a) HNO3, H2SO4 (b) Br2, FeBr3Which of the following ethers would be obtained in greatest yield directly from alcohols?
- Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict themajor products of the reactions of naphthalene with the following reagents.(a) HNO3, H2SO4 (b) Br2, FeBr3 (c) CH3CH2COCl, AlCl3Rank the compounds in each group in order of increasing reactivity in nucleophilic acyl substitution. CH3CH2CO2H, (CH3CH2CO)2O, CH3CH2CONHCH3Describe how each of the following compounds could be synthesized from the given starting material.