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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- 1, part A) In the reaction below, draw all of the possible products. 1, part B) For all the products you have drawn, draw their corresponding carbocations while also identifying if each is 1o/2o/3o carbocation. In addition, starting from alkene - provide complete accurate arrow-pushing mechanisms of each carbocation formation. 1, part C) In part B, circle the carbocation which is *most* stable, indicate why.Reaction of 2-methyl-2-butene (above) with HBr might, in principle, lead to a mixture of two alkyl bromide addition products. Draw these two alkyl bromides.Complete the multistep mechanism for the formation of each of the possible monochlorination products from reaction of 2,2,4,4-tetramethylpentane with chlorine in light. Initiation step in the presence of light. Use curved arrows to show the mechanism of the propagation steps below. (Click on the blue box to toggle through four possible arrow choices.) a) Formation of the 1-chloro-2,2,4,4-tetramethylpentane b) Formation of the 3-chloro-2,2,4,4-tetramethylpentane. H- CH3 CH3 HaC CH3 CH3 |CH3 Hас Cнs НаС, CH3 -CH2 CH3 H CH2 Нзс. CHа CH3 CH3 CHa Нзс CHa CH3 CH3 CHa CH3 CH3 CH3 Нс- Нзс CH3 CH3 H CH3 CH3 CH3 CH3 ~сна CHa ~Cн сн3 сн CH3
- 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. 1Give 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.Discussion questions: Which regioisomer(s) of methylnitrobenzoate do you expect and why? Summarize your data that identifies the regioisomer corresponding to your major product. Draw your product and number the ring, according to UPAC nomenclature rules. - My major product was meta nitromethylbenzoate The reaction involved methylbenzoate 0 HN H₂SO recating with H2S04 and Hno3 THE REACTION -
- Write equations that show the mechanism of the dehydration of 3-pentanol. Two possible products can form, show both and determine which is the major product.Show and label the mechanism for the SN1 reaction using the generic chemical species and electron movement. Notice that the reaction does not include a negative charge on the nucleophile.or 2. Provide the major product(s) for the reactions below. Clearly indicate the stereochemistry in your structures where appropriate. Where more than one stereoisomer is formed you only need to draw one of the stereoisomeric products. Other stereoisomers should be indicated by writing, "+enantiomer" "+diastereomer", as appropriate. Check the boxes on the right to indicate whether the reaction product solution would be optically active ([a]o * 0) or not optically active ([a]o = 0). Under the checkboxes give your rationale for the selection using one of the following: achiral, racemic, meso, single enantiomer, mixture of diastereomers. a) b) c) H OH Jones reagent OH OH Na₂Cr₂O7 H*, H₂O Dess-Martin Periodinane CH₂Cl₂ [a]o #0 [a] = 0 [a] #0 [a]D=0 [a] #0 [a]D=0