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Solved in 4 steps with 2 images
- 6. Identify the best reagent(s) for this reaction. (see attached screenshot). a. H2SO4, HgSO4, H2O b. 1. Disiamylborane, 2. HO–, H2O2 c. K2Cr2O7, H+ d. NaOCl e. H2, PdShow the reaction mechanism for the formation of:a. RCONH2 from the reaction of RCOOR’ with NH3For the nitration of a monosubstituted benzene, which substituent, when attached to benzene, produces the fastest reaction rate? —Br —CH3 -OCOCH3 —OCH3
- How does changing the alkyl halide from CH3CH2Br to (CH3)2CHBr affect the rate of an E2 reaction?Which mechanism gave the main product in the reaction shown in Figure 8? * A- SN1 B- SN2 C- E1 D- E2Which reactions will proceed faster in a polar, aprotic solvent? (CH3)2CHCH2I+Na+N3−(CH3)2CHCH2I+Na+N3− (CH3)3CBr+HSCH2CH3(CH3)3CBr+HSCH2CH3 CH3CH2CH2Br+Na+CN−CH3CH2CH2Br+Na+CN− (CH3)2CHOSO2CH3+HOCH(CH3)2
- What is the major product of the reaction below? What is the mechanism? (See the image) a. 2-bromo-3-methylpentane, SN2 b. 3-methoxy-2-methylpentane, SN2 c. 3-bromo-2-methylpentane, SN2 d. 2-methoxy-3-methylpentane, SN2A carbocation intermediate is central to which of these reaction types? E1, E2, SN1, SN2 ? Choose 1Plan out a proposed mechanism for the “new” reaction below.
- 2.Show the 2 step reaction Mechanisms of the compound belowFor each reaction indicate the predominant mechanism: SN1, SN2, E1, or E2Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- ΔH=-75 kJ/mol Rate = k [CH3CH2Br][CH3COO-] Which reaction energy profile would be the best representative of the data provided?