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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)?out of 4, which numbers will readily undergo an sn1 reaction?Arrange the following group in order of increasing priority. Q) -CH3 -H -Br -CH2CH3
- Rank the following groups in order of decreasing priority. −COOH, −CH2OH, −H, −CHOIn 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:First Writedown which reaction it is? SN1, SN2, E1? Write a stepwise mechanism for the following reactions showing ALL intermediates. Use curved arrows to symbolize the flow of electrons to show how each of the intermediates and product are formed. Show all necessary lone pairs and formal charges.
- Show how HC ≡ CH, CH3CH2Br, and (CH3)2CHCH2CHBr can be used to prepare CH3CH2C ≡ CCH2CH2CH(CH3)2. Show all reagents, and use curved arrows to show movement of electron pairs.Please write down the resulting products. How can I know which of the two substituents already present is more strongly conducting in the case of double-substituted benzene? Is generally ortho preferred to para? In the example of OH and NH2 both otho,para conducting. So are there three possible products?Could someone help me with ranking these with how reactive they would be with an SN2 reaction? Thanks :)
- Show how HC≡CH, CH3CH2Br, and (CH3)2CHCH2CH2Br can be used to prepare CH3CH2C≡CCH2CH2CH(CH3)2. Show all reagents, and use curved arrows to show movement of electron pairs.Draw the products of the SN1 reaction below and use wedge-and-dash bonds to indicate the stereochemistry of any stereogenic centers.Explain why the trifluoromethane sulfonate (TfO-) ion is a better leaving group than the methanesulfonate (MsO-) ion.