Please explain with mechanism I'm so confused what mechanism I should have to use.
Step 1: elimination of TsOH and formation of allyl cation with
methoxide.
Step 2: methoxide ion attack on the cation to form the product
1.
Step 3: in another pathway, methoxide ion can deprotonate the
cationic molecule to form a diene, which is the second product
Please explain with mechanism I'm so confused what mechanism I should have to use. Part III...
Part III - Mechanism (14 marks] A. Use the curved arrow notation to draw the step-wise reaction mechanisms that account for the formation of the products shown in the transformation below. All reactants are shown. (8 MARKS] MeOH осна + -TsOH
A. Use the curved arrow notation to draw the step-wise reaction mechanisms that account for the formation of the products shown in the transformation below. All reactants are shown. (8 MARKS] OES=0 MeOH w осн. -TsOH
I need some help with part b in the question please (a) Propose a one-step mechanism using curved arrow notation for the formation of styrene oxide from styrene using MCPBA, as shown below. (b) Propose a step-wise mechanism using curved arrow notation for reaction of styrene oxide with (CH_3)_2 CHNH_2 that includes the structure of the expected product. To simplify the mechanism, do not show formation of enantiomers.
Part III - Mechanism cont'd B. Using curved arrow notation, draw the reaction mechanism and predict the product the reaction below. Show all reaction intermediates and account for stereochemical requirements. [6 MARKS] or EtoNa / EtOH ? OTS Heat
Please answer all two questions and please explain! I'm completely lost at the moment and I'm not sure how to solve it. Please do it step by step if possible. 6. (12 points) Provide products for the reactions shown below. Draw all possible stereoisomers and indicate if the products are achiral, chiral, racemic or meso Br2 Нао Н Br2 CCI 7. (15 points) Predict the major product for the following acid catalyzed hydration reaction, and drawa detailed mechanism using curved...
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...
Name: Aexab yard Chapter 10: Mechanisms 1. Provide a mechanistic explanation for the formation of the observed products in the following cat. H50 heat 2. Draw an arrow-pushing mechanism to justify the following transformation. OH heat Write a plausible arrow-pushing mechanism for the reaction depicted. Make sure that you account for the stereochemistry shown. 3. Br Br2 MeOH OMe
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. 6. (10 points) Provide products for the reactions shown below. Draw all possible stereoisomers and indicate if the products are achiral, chiral, racemic or meso. Вrz Hао 1) ВНз-THF 2) H,О, NaOH 7. (10 points) Draw a detailed mechanism using curved arrow notation for the reaction shown below. H2SO4...
Started to work this problem out but i've gotten confused. May someone please show me the corrct mechanisms to complete these questions? Thank you. 1. Give a complete curved-arrow mechanism for the reaction shown. Draw in any missing product structures. one other stereoisomer (draw in structure) 2. The ether shown, when reacting with excess HI gives the products shown. HO excess a. Give the complete curved-arrow mechanism for this reaction. b. Explain in about two sentences why this result is...
PROBLEM 5. Reaction Mechanism 1. Propose products (major/minor) and provide a detaile reaction mechanism to account for the formation of the major product. Use curved arrow notation to indicate electron flow. Also, draw a structure of the transition state that accounts for the formation of the major product HЕr он 0° C major minor transition state corresponding to the major product of 20 points