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Question 12 - 6 pts. Homework What is the major product when 2-bromo-2-methylpentane reacts with potassium...
what major E2 product would form on the reaction of (2S,3R) 2-bromo-3-methylpentane with base? QuesLIUI What major E2 product would form on reaction of (2S,3R) 2-bromo-3-methylpentane with ba CH3 O (Z) 3-methylpent-2-ene (E) 3-methylpent-2-ene (3R) 3-methylpent-1-ene (Z) 3-methylpenta-1,3-diene
QUESTION 2 What major E2 product would form on reaction of (2S,3R) 2-bromo-3-methylpentane with base? |||11111 CH3 A. (Z) 3-methylpent-2-ene B. (E) 3-methylpent-2-ene C. (3R) 3-methylpent-1-ene D. (Z) 3-methylpenta-1,3-diene
What are the mechanisms and major/minor products when 2-Chloro-2-Methylbutane reacts with A.) Potassium Hydroxide in 1-propanol+Heat B.)Potassium tert-butoxide in tertbutyl alcohol+heat I know they proceed via E2 reaction mechanism but need help figuring out the steps and the major and minor products. Also if you could offer a brief explanation of why the mechanism reacts the way it does I would really appreciate it. Thank you!
What is the major product resulting after heating 1-bromo-3-methylpentane with 2M sodium hydroxide What is the major product resulting after heating 1-bromo-3-methylpentane with 2M sodium hydroxide: Select one: a. 3-methylpent-2-ene O b. 3-methylpent-1-ene O C. 3-methylpentan-1-ol O d. 3-methylpentan-2-ol e. There is no reaction
Question 25 6 pts Complete the 2 step synthesis below that converts 2-bromo-2-methylpentane to 3-bromo- 2-methylpentane. (A) will represent your reagents for the first reaction. (B) represents the product of the first reaction (and the starting material of the second), while (C) represents the reagents for the second reaction. You will write your answers out and then submit them via a file upload. You can either recreate the format shown below, or just simply list A,B, and C along with...
A) Reaction of 3-bromo-3-methylpentane and H2O and heat Draw the major product formed when the structure shown below undergoes substitution in H2O with heat. B)Substitution reaction of 3-bromo-3-methylpentane and CH3OH Draw the major product formed when the structure shown below undergoes solvolysis in CH3OH.
7. Shown below are the major product formed and the proposed mechanism when 1- methylcyclohexanol reacts with 85% H3PO4 at 150 °C. Name all curved arrows shown in each step as either "lone pair to bond" or "bond to long pair". Specify the atom that donates/accepts the lone pair. [1 Mark] Step 1 -H O ro-H + Ho + H2O H H Commons Kagamo Step 2 + H2O Step 3 = + H,PO. H HAPO Zaitsev product 6. Given below...
organic chemistry Question 6 Choose the final, major product for the following reactions. cyclohexanol reacts with: a) PC13/ pyridine b) гон c) HBr / heat d) tert-butoxide e) BH3 / THE f) OH, H202, H20 1. bromocyclohexanol O2. cyclohexane 3. cyclohexene 4. cyclohexanol
When 1-bromobutane reacts with sodium tert-butoxide (the conjugate base of tert-butyl alcohol) the major product is the elimination. Is this E1 or E2? Show the product Based on the information given in the problem, what was the key factor that changed the changed the major product from substitution to elimination?
When 3-bromo-2,2-dimethylbutane is treated with potassium tert-butoxide, a single product, A, having the formula C6H12 is formed. When 3,3-dimethyl-2-butanol is treated with sulfuric acid, the major product, B, has the formula C6H12. Given the following NMR data, what are the structures of A and B?Write reactions for the formation of A and B and draw a splitting diagram for the protons at 4.82, 4.93, and 5.83 ppm in compound A1H NMR of A: 1.01 (s, 9H), 4.82 (dd, 1H, J = 10, 1.7 Hz), 4.93 (dd,...