please answer only the widely applicable knowledge, not data type questions as most of are that are shown
please answer only the widely applicable knowledge, not data type questions as most of are that...
draw a mechanism for methyl 3 benzoate
2. For the nitration of methyl benzoate: Which product did you get? What evidence doyou have for this? Wasyourproduct pure? Whatevidence do you have for this? Explain your a. b. evidence. c. Draw the mechanism for the product you got. d. Calculate percent yield. Show your work
Please only answer parts that dont require all of my data (
mechanism of bromination and what to look out for as far as
purity)
For the bromination of acetanilide: a. Which product did you get? What evidence do you have for this? b. Was your product pure? Whatevidence do you have for this? Explain your evidence. c. Draw the mechanism for the product you got. d. Calculate percent yield. Show your work.
3. For the bromination of acetanilide: a. Which product did you get? Whatevidence do you have for this? b. Was your product pure? Whatevidence do you have for this? Explain your evidence. C. Draw the mechanism for the product you got. d. Calculate percent yield. Show your work.
For the nitration of methyl benzoate:
a. Which product did you get? What evidence do you have for
this?
b. Was your product pure? What evidence do you have for this?
Explain your evidence.
c. Draw the mechanism for the product you got.
For the bromination of acetanilide:
a. Which product did you get? What evidence do you have for
this?
b. Was your product pure? What evidence do you have for this?
Explain your evidence.
c. Draw the mechanism...
Post Lab Questions for Nitration of Acetanilide, Nitration of Methyl Benzoate, Nitration of Phenylacetonitrile, Nitration of Phenol. 1. What product(s) do you expect to be formed in the nitration of phenol? Why? 2. All three of the nitrophenols have boiling points well above 200°C. Explain clearly why it was possible to distill something with such a high boiling point when the temperature of the distillate never rose much above 100°C. 3. What product did you actually obtain in the distillate?...
1. Write a detailed mechanism for the reactions of phenylmagnesium bromide with methyl benzoate which produced the conjugate base of triphenylmethanol. 2. Assume that we ran this reaction with 1.0 g Mg, 4.5 mL bromobenzene, and 2.3 mL methylbenzoate. If you got 2.15 g of product calculate your percent yield for this reaction. (just do number 2 please)
Please and all two questions
and explain how you got to your answer. I'm really lost and I have
an exam in 7 days! A step by step would be appreciated.
9. (20 points) For the reaction shown below, a) predict the product b) draw a detailed mechanism using curved arrow notation c) draw the coordinate energy diagram d) label the reactants, intermediates and products on the energy diagram e) Which step is rate determining? Why? a HBO Reaction Progress...
Analysis Questions 1. Given the structure of an aldehyde and a ketone, predict the structure of the reaction product. Use the table below to practice and to predict the possible products your class synthesized. HẠC CHỊ acetone cyclopentanone benzaldehyde Product #1, m.p. 113 °C Product #2, m.p. 189 °C NA trans-cinnamaldehyde Product #3, m.p. 144 °C 2. Include the IR spectrum of your product. Label important peaks with corresponding functional group. 3. Include the melting point your product. 4. Draw...
1. Derive your own fact pattern or case that demonstrates your knowledge of skimming and answer the following questions - 10 points What piece or pieces of evidence do you see as most proving your case? Why? 10 points. After you have discussed the evidence do you believe you have enough in terms of totality of the evidence as as whole? Why? 10 points. 2. Cash Larceny - do the same as in # 1 above. 30 points.
please answer only questions 2 and 4. thank you.
Questions 1. Suggest a mechanism for the basic hydrolysis of methyl benzoate. 2. What is the general formula for a soap? Write an equation for the reac- tion of ethyl stearate and sodium hydroxide. Explain briefly how a soap works. 3. Is sodium hydroxide a catalyst or a reactant? Explain. 4. Why is basic hydrolysis irreversible? 5. Provide the hydrolysis products in the reactions below: a. O II C- OCH +...