2) Predict the major product(s) of the following reaction. Also, write the mechanism for the transformation. Br LDA diisopropylamine to (abubong nojam 9 tailben
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- Why do you suppose ketone halogenations in acidic media are referred to as being acid-catalyzed, whereas halogenations in basic media are base-promoted? In other words, why is a full equivalent of base required for halogenation?GIVE A COMPLETE MECHANISM FOR THE FOLLOWING REACTIONa) Provide the complete mechanism for the following reaction. MeO CH;CH2NH2 CH;OH b) Design a synthesis for this primary amine starting from benzene. CH2CH2NH2 но
- The dehydration of pinacol can take place via two mechanisms, leading to the formation of thetwo products shown below: a) Draw detailed mechanisms for the formation of both products, including any resonancecontributors. b) Briefly explain why pinacolone formation is favored.May you please help me with this ochem question?The treatment of a nitrile with cyanide yields an a- aminomalononitrile, as shown here in the reaction. Provide a detailed mechanism for this reaction. CN NaCN EN HCN -NH2 ČN An a-aminomalononitrile
- Give detailed Solution with explanation neededWhich of the following will be the dominant product of the dehydration reaction shown? H;PO, H2O. A но (A) (B) (C) (D) Compound B Compound C OCompoundD OCompound A nintc)Use the reaction given below to answer the following questions. A CH₂OH B H₂O+ C + CH3NH3* D a) What are the approximate pKas of compounds A and B? b) The reaction given above is irreversible. Give a detailed explanation of the reaction and reaction mechanism. Your explanation should indicate your knowledge of the reactivity of carboxylic acid derivatives.