What would be the major and minor product of (1E, 3E, 5E)-1-methoxyhepta-1,3,5-trien with the addition of HBr. Draw both products and explain why each product is either major or minor. *justify it*
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What would be the major and minor product of (1E, 3E, 5E)-1-methoxyhepta-1,3,5-trien with the addition of HBr. Draw both products and explain why each product is either major or minor. *justify it*
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- The following compound readily eliminates CO; to form a conjugated six membered ring. (a) Complete the reaction with drawing the possible structure and (b) explain why this reaction goes steadily.Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the product of this elementary step in an SN1 mechanism. Include all lone pairs. Ignore stereochemistry. Ignore byproducts.Complete the mechanism of hydration of alkene below. Please follow curved arrows to predict the resultingstructures in each step.
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the product of this elementary step in an SN1 mechanism. + Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore byproducts. Nal <Show how to accomplish the following alkylation. (a) Step 1 (i) Specify the reagent used in this step. (ii) Draw the structure of the intermediate formed in this step, compound A. (B) draw the structure of the reagent needed for this step. (C) specify the reagent used in step b C Show how to accomplish the following alkylation. [References] Step 1 Step 2 compound A Step 3 CO₂Et (a) Step 1 (i) Specify the reagent used in this step. (ii) Draw the structure of the intermediate formed in this step, compound A. 16) Write the mechanism (two propagation steps only, starting with the bromine radical in the first step and using Br2 in the second step) and that would explain how the following two products are produced. (Hint – the allylic radical is resonance stabilized.) Br Br NBS
- Give a detailed reaction mechanism for the reaction expected to occur when 2-bromo-2- methylpentane is heated with sodium methoxide. • Draw clear structural formulas of all relevant species and use curved arrows to represent electron flow. Indicate which step is likely to be rate determining.4. Which stereoisomer is the major product for the following reaction? Fill in the missing brackets with the key intermediate/transition state that leads to the preferred stereoisomer. Briefly explain (one sentence or bullet point) your selection. Br₂ key intermediate Br Br Br && or BrThe molecule, 2-bromo-1,3-diethyl-1,4-dimethylcyclohexane undergoes an SN1/E1 reaction in the solvent ethanol. i) Draw the intermediate resulting from the first step of this reaction. ii) Draw the two most favorable intermediates resulting from carbonation iii) From the intermediate(s) in (ii) draw all the possible E1 products and circle the product(s) that is(are) most favorable. iv) Name the most favorable product(s). v) Draw an SN1 product from an intermediate in (ii).
- Please help me to show the major products and complete the mechanisms with proper arrow pushing notation.Provide a stepwise mechanism to explain the formation of the products in the following reaction. Remember to show electron flow using the appropriate type of arrows please!!!! (draw it out) You do not need to include a termination step.Give a detailed reaction mechanism for the reaction expected to occur when 2-bromo-2-methylpentane is heated with sodium methoxide. Draw clear structural formulas of all relevant species and use curved arrows to represent electron flow. Also indicate which step is likely to be rate-determining. The answer you sent before will be used for this question.