3. Give the complete electron flow of the SN1 reaction, be sure to clearly show the electrons that are flowing. Br + CH;CH,CH,CH,OH, Bĩ CH3CH2CH2CH,OH 4. Give the complete electron flow of the E1 reaction, be sure to clearly show the electrons that are flowing. Br + HO Br CH3CH2CH2CH2OH
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- What are ALL of the products of buta-1,3-diene and bromine water? I know how to get to the major product (bromine and OH both to the left of the double bond) but don't know how to get to the minor product (bromine to the left, OH to the right)?Construct an efficient three-step synthesis of 1,2-epoxycyclopentane from bromocyclopentane by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used.Why is tertiary carbocation most favored for Sn1 reactions?
- In parts 1 and 2 draw the two organic products of this reaction, showing any nonzero formal charges. Then, in part 3 answer the question regarding purification of the reaction mixture. 1. Draw the product with the higher molecular weight here: 2. Draw the product with the lower molecular weight here:What are the reagents needed to get the product? For #3, what would be the product after Br2, light reaction? For the second part of #3, what reagents are needdd to react with that previous product in order to get the final product?What has the correct product in this synthesis reaction and explain why? BaO+SO2=BaSO3 or BaO+SO2=BaSO4
- Assume that 2-chloropropane reacts with CN− in an SN2 reaction. Use the JSME editor () to draw the structure of the substitution product of the reaction. The guide on how to draw your structure can be found here Important Note: When drawing the structures in the JME editor please adhere to the following formats: 1. If the nucleophile is OH−, DO NOT manually add the "H" to the final product 2. If the nucleophile is CN−, be sure to include the appropriate bonding between the C and N in the final product1.)How is this reaction is carry out ? Show all the steps please arrows and all the movement of electrons. 2.)Show the Jones intermediary1, 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.
- Any help with this would be great! Explanations definitely welcome, thanks in advance for any help:) What is the major product of the reactions?Construct a three‑step synthesis of 1,2‑epoxycyclopentane from bromocyclopentane by dragging the appropriate formulas into the bins. Note that each bin should hold only one item, and not all of the given reagents or structures will be used. Reactant −→−−−−reagent 1 →reagent 1 Step 1 product −→−−−−reagent 2 →reagent 2 Step 2 product −→−−−−reagent 3 →reagent 3 Final productIn the reaction series below, write down the appropriate reagents that can be used where there are question marks.