(A) phenyl methyl amine is
better nucleophile than ammonia it again react with benzylbromide
and not available as a product, or available as very por
product.
(B) The working synthesis for benzylamine is given by reacting benzylchloride with hexamethyleletetramine .
9) 18 points total. A) Please explain why the reaction below will not work. We will...
A) Please explain why the reaction below will not work. We will take points off if you use more than 2 sentences in your explanation! B) Please propose a synthesis of the above product amine that will work.
2. The following reaction will not work. Please explain why. cat. H-Br NH; solvent NH2 3. Use your knowledge of mechanisms to predict the product for each reaction: LiAlH4 → ????? LiAlH4 ????
3. Based on your answer in 2. select the most likely reaction pathway. Explain how the substitution mechanism forms the product structure(s) shown. 2points А, H Br off and add NH toi O position because it Would Rick Ph Ph Ph- B H NH2 Ph Ph + NH 4. Identify the reaction components and solvents as more soluble in the aqueous (A) or organic (O) layer during separation of substitution and protonation steps. 3 pts Br HN НN CIO NH3...
(10 points) Draw the correct product for the reaction below. For step 2, draw the reaction mechanism. Be sure to include important intermediate compounds, electron flow arrows, and formal charges for full credit. ОН 1. SOCl2, pyridine 2. CH3NH2 (10 points) Fill in the boxes with the missing starting material, intermediate products, reagents, and/or products. Then for each reaction draw the reaction mechanism with Correct electron flow arrows if appropriate or intermediates and correct formal charges. -OH -NH2 NH (10...
My teacher is that A is not the major product. please explain
why and what would be the major
22) (9 points) For the following reaction: a. (5 points) Draw a complete and detailed mechanism for the process shown below to form compounds A and B. mention whether it is initiation, propagation or termination. b/ (2 points) Explain why this reaction gives a mixture of compounds A and B and does not give compound C c. (2 points) Which product...
please explain why the answer is the answer step by step
Retrosynthetic Analysis Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (ie. ortho/para products) then indicate...
9-11
9. See the figure below for 9 i-lii (22 points total). 100 Total Primary response Secondary response Antibody concentration in serum, units per ml Total IgG 0.1 IgM IgG IgM Klag 0.01 1 2° Ag 1° Ag Time after immunization 9 i) During the lag period in the graph above, why are there no antibodies being produced? (8 points) 9 iii) In the secondary immune response to an antigen (Ag), IgG has greater specificity for the antigen than in...
please explain why
Later in the course, we will compare the halogenation of differently substituted carbons, comparing reactions like the ones below. Which of the following reactions has a more exothermic heat of reaction (AHº)? A) ~ + Br-Br + H-Br „Br + H-Br B) + + Br-Br A. Reaction A has a more exothermic heat of reaction (AH) B. Reaction B has a more exothermic heat of reaction (AHº) | C. Both reactions have the same heat of reaction...
7-9 please!
4 7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) H Acidity of one pf the H's shown H H 8. For the reaction show a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control" product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures...
Please answer question 4 with a full explanation.
4. (9 points) Multi-step synthesis. Devise a synthesis for the target molecule starting from benzene and small alcohols with no more than two carbons. You can use any inorganic reagents necessary target 5. (10 points) Analysis of 'H NMR spectrum. Below is the 'H NMR spectrum of the product from this week's experiment.