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- Draw the products of attached SN2 reaction and indicate the stereochemistrywhere appropriate.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?Hello, thank you this was very helpful. However, i still dont completly understnad how to determin and explain why the isomer of B is the major product. Could you explain this in a differnt way?
- (need answer in step by step) Deaw major product of followinv reavtion, make sure to draw enantiomers if expectedSo far I've gotten feedback "Carboxvlic acids are poor electrophiles but can be converted to acidderivatives with activation by DCC. Review the reagents and conditionsprovided to identifv the nucleophilic addition-elimination reaction that willoccur keeping in mind any stereochemical or regiochemical preferences."plz write a plausible mechanism with clear arrow pushing.
- how we convert gamma bisabolene into 10 alpha chamigrene . exaplain with proper mechanismCan u help pls with a mechanism for one from the three reaction thank uDraw the equilibrium chair confirmation of cis1-chloro-3-methylcyclohexane. Interpret the E2 elimination, and draw the structure of the product!
- Bromide Bhas normal activity (for a secondary bromide) towards SN1 substitution, but A has much higher reactivity and Chas much lower reactivity.Interestingly, reduction of the complex shown above mostly gives thealcohol enantiomer shown below after workup. a. Draw the other minor diastereomeric alcohol product. b. Briefly explain the diastereoselectivity of the reduction – why is oneenantiomer heavily favored? Draw a structure or structures to support youranswer.Identify the organic functional groups and reaction type for the following reaction.The reactant is a(n)a. beta pyranoseb. beta furanosec. alpha pyranosed. alpha furanoseThe product is a(n)a. alpha furanoseb. alpha pyranosec. beta furanosed. beta pyranoseThe reaction type is:a. oxidation (benedict's)b. esterificationc. mutarotationd. reduction (hydrogenation)e. hemiacetal formation