5. Identify the reactants needed to convert acetone to each product. 6. Propose a mechanism for each:
5. Identify the reactants needed to convert acetone to each product. 6. Propose a mechanism for...
Please help with this because this is a practice exam and my professor hasn't posted the answer key. I have worked on it but I have nothing to compare it to and work with. Thank you. Chapter 14: 1. Draw the following: 2-methylheptan-3-one 2-methylhexanal 2. Name the following: 3. Identify the reactants needed to convert acetone (left) to each product (right): 4. Propose a mechanism for each: Chapter 15 and 16: 5. Draw the following: a. Propyl ethanoate b. Propyl butane thioate c. N, N-dimethyl pentamide d....
2. Predict the product and propose an appropriate mechanism for the following trans Identify whether the faces of the carbonyl are homotopic, enantiotopic, or diasto pts) e following transformation. topic, or diastereotopic. (6 W 2.4,0 ado color 3. Predict the product and propose an appropriate mechanism for each of the following transformations. (14 pts) O C T velog 2. H20 Alle loro ode Sota som motulostinwant
NAME Question 1 Organic Chemistry assignmen Propose the reactants and mechanism to obtain the following product (not necessarily major). NH NHa 2 STEPS OH 1STEPS cEN 2 STEPS
Problem 5: Propose a synthesis that would convert the starting material to the desired product. Problem 6: Propose a synthesis that would convert the starting material to the desired product. OH
Identify the products of the following reactions and propose a
mechanism for its formation. Please explain each step i.e.
protonation, deprotonation, loss of leaving group, or nucleophilic
attack and describe what kind of reactions they are. Include BOTH
major and minor products. Thank you in advance.
NaOEt EtOH Me H0 2 CI 6 12 CI acetone
NaOEt EtOH Me
H0 2 CI 6 12 CI acetone
5. Identify the reagents you would use to convert cyclohexanone into each of the following compounds NOZ 6. Draw a plausible mechanism for the following transformation:
2. Provide missing conditions, reactants in the following synthesis. Propose the structures for Products A, B and C. Note: each step consists of more than one transformation. Step 1 in slope fin Step 2 Hint: you can use Br 1. H', ethylene glycol, heat 2. NaOH/H, O, heat 3. H30* Product A Step 3 HCl dilute Product C Product B 1. PhMgBr, ether 2. H20 acetone Step 1: Step 2: Step 3: 3. Show the full mechanism of Step 3...
Predict the product of the reaction mechanisms. Identify the electrophile and nucleophile in each reaction. Propose a mechanism for each reaction below. This means show curved arrows. You may want to fill in any nonbonding electrons. Show an example of each of the following types of reactions and explain why it is that type: Addition elimination Rearrangement Substitution
Propose a mechanism for the follo heat Br Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron flow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond should be created H-Br: Cl H-Br: H20
1. Propose a mechanism for the formation of the given product: (6 po HT H2O