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- Predict the main product of the reaction in Figure 10. * A B C D The main product of the reaction cannot be predicted.Predict the product, draw the mechanism, and plot the reaction coordinate diagram for theE1 reaction.The replacement of CH3OH to dimethyl sulfoxide, DMSO (CH3)2S=O) as a solvent in the substitution reaction below results in what?
- Complete the following reaction equations :(i) C6H5Cl + CH3COCl →(ii) C2H5NH2 + C6H5SO2Cl →(iii) C2H5NH2 + HNO2 →Do the reactions below proceed in good yield from left to right as shown? Please fill in Yes or NoConsider the series of the trans effect: CO, CN-, C2H4 > PR3, H-, CH3- > C6H5- > NO2-, SCN-, I- > Br- >Cl- > py > NH3 > H20 What would be the major product of the following reaction? Select one:
- M 6 write the principal product in a, c & e and the neccesary reactives for b, d & f in the following reactions :Which of the following reactions result in a positive ∆ Ssys? A. Pb(NO3)2 (aq) +KCl (aq) ---> PbCl2 (s)+ KNO3 (aq) B. HCl (g) + H2O (l) ---> HCl (aq) C. H2 (g) + I2 (g) ---> 2HI (g) D. 2H2O (g) ---> 2H2 (g) + O2 (g) E. H2O (g) ---> H2O (l)Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?
