Complete the mechanism for the reaction of butanone with NaBH4 followed by the addition of aqueous acid.
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Complete the mechanism for the reaction of butanone with NaBH4 followed by the addition of aqueous acid.
Complete the mechanism for the reaction of butanone with NaBH4 followed by the addition of aqueous acid.
complete the mechanism Complete the mechanism for the reaction of butanone with NaBH4 followed by the addition of aqueous acid.
Complete the mechanism for the reaction of butanone with NaBH4 followed by the additin of aqueous acid.
Maput Complete the mechanism for the reaction of butanone with NaBH, followed by the addition of aqueous aciu. 1. NaBH CH,COCH, 2.H, o Add curved arrows to show the mechanism of the first step of the reaction. Draw the charged organic intermediate product. Include nonbonding electrons and charges. Omit the counterion. SEO: continued below Na BH Draw the final product. H, Previous continued Hint Check Answer Next Exit ►
Complete the mechanism of the reaction between benzaldehyde and dimethylamine in acid followed by introduction of a hydride reducing agent. Add any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. Note the use of a generic base B:, which represents another amine in solution that acts as a shuttle for the added acid Continued
Provide a detailed, stepwise mechanism for the acid-catalyzed reaction of 2-butanone with ethylene glycol (HOCH_2CH_2OH) to produce an acetyl.
Provide a detailed, stepwise mechanism for the acid-catalyzed reaction of 2-butanone with ethylene glycol (HOCH2CH2OH) to produce an acetal. HC. CH HCL HOSH HCC oc 다
Complete the mechanism for the reaction of butanone hydrate to produce butanone under conditinos of NaOH in water. A reversible reaction takes place, but we will just draw the arrows for formation of the carbonyl in this problem. :0: Hö: OH NaOH H2O :0: Step Step H-Ö ÖH OH : HT Two One :0H Draw the arrows for the 3-step mechanism in formation of the hydrate. (This would not build up and be isolated, but show how it would form.)...
QUESTION 4 [1,2- versus 1,4-Addition Reactions] 4.1 Propose a detailed mechanism for the reaction of 2-butenal with ethynylmagnesium bromide in dry THF followed by quenching with dilute aqueous acid. (5) 4.2 Propose a plausible mechanism for the reaction of 1,3-diphenyl-2-propen-1- one with potassium cyanide in ethanol followed by aqueous work-up. 1 (5) 4.3 Predict and draw the structure of the product of the reaction of 2-methyl-1,3- cyclohexanedione with methyl vinyl ketone (3-buten-2-one) in methanol in the presence of potassium hydroxide....
Show the reaction of 2-methyl-2-pentene and (CF3CO2)2Hg/CH3CH2OH followed by NaBH4. Show the products of the reaction of your ether in #4 and acid.