what would you expect your final product to be if.....?
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what would you expect your final product to be if.....? ab queStiun s wnot would yon...
Draw the structure(s) of the major organic product(s) you would
expect from reaction of m-toluidine (m-methylaniline) with HNO2 and
H2SO4 followed by KCN and CuCN
Draw the structure(s) of the major organic product(s) you would expect from reaction of m-toluidine (m-methylaniline) with HNO and HjSO followed by KCN and CuCN. You do not have to consider stereochemistry. . You do not have to explicitly draw H atoms. y will not be considered in the grading. Include counter-ions, e.g., Na,I, in...
What is the final product for the following reactions?
What is the final product for the following reactions? (S pts) 2. 1DBr, FeBr 2) H2SO4 HNO 3) H,SO, (fuming) 1)H,SO, HNO 2) HSO, (fuming) 3) Br. FeBr.
1. After filtering your final product, you find that your product is still wet, but you proceed to take a melting point anyways. The literature melting point of luminol is 319 °C. What do you expect the melting point of your luminol to be? What would you expect the yield to be? Would it be an accurate yield? 2. While going to conduct the chemiluminescence test, you forgot to dilute Solution A. What do expect the effect of your chemiluminescence...
2. What product would you expect from the following
reaction?
2. What product would you expect from the following reaction? ÇOCH H+ CO CHE A. in ÇOCH3 B CO.CH ÇO,CHE D. CO,CHE E
f. From your knowledge of the radical addition mechanism, what product would you expect from the treatment of 1,3-butadiene with HBr in peroxide containing ether. Support your answer by showing the mechanism for the reaction and the role played by the peroxide. (6 pts)
Draw the organic product(s) you would expect from the following reaction. Draw the organic product(s) you would expect from the following reaction. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms.
1. After filtering your final product, you find that your product is still wet, but you proceed to take a melting point anyways. The literature melting point of luminol is 319 °C. What do you expect the melting point of your luminol to be? What would you expect the yield to be? Would it be an accurate yield? 2. While going to conduct the chemiluminescence test, you forgot to dilute Solution A. What do expect the effect of your chemiluminescence...
4. What product(s) would you expect from the reaction of 1,4-hexadiene with NBS? What is the structure of the most stable radical intermediate? (5 marks)
What product(s) would you expect from the following reaction? CH2 NBS CCl4 3
3. Given what you now know, what product(s) would you expect to isolate from this reaction? Y +Na + Nao + - Br (NaOf-Bu) Specify how each of the following would affect the rate of the reaction. a. Increase the concentration of the base. b. Decreasing the concentration of alkyl halide. 3. Predict the product(s) for each of the E2 elimination reactions below. major product for each. heat Br NaOCH3 heat