Он 5-со но-в + ножон acetonitrile 'B' rt, 4h pinacol

Q: J. Provide detailed (arrow pushing) mechanism for the following reaction, draw all important…

A: Lewis acid: Lewis acids are electron pair acceptors. These have atoms either having partial/complete…

Q: (SYN) Show how each of the following Grignard reagents can be synthesized from an alkyl, alkenyl,…

A: Grignard reagent is a class of organometallic compounds having molecular formula of alkyl magnesium…

Q: Is it possible to have tautomerism of pyrrole in Equibilirium condition?? If no, then Why? and in…

A: In the given question we have to predict whether tautomerism is possible in pyrrole in equilibrium…

Q: What elementary step is represent by the curved arrows shown below? 00 0=< + RH Proton Transfer…

A: Answer:Any specie that accepts the proton (H+ ion) in its solution is called as Bronsted-Lowry base…

Q: Which ketone, E or F, do you think has the more stable T system? Why? Hint: Consider various…

A: The compound E and F contain a conjugated ring with a carbonyl group. In the carbonyl group, the…

Q: Kindly Draw the Full mechanism (with electron pushing and formal charges) for the Wolff-kishner…

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Q: A pair of diastereomers is each individually mixed with a strong base, and for both, an E2 reaction…

A: Diastereomous are ------Now if there two inomous undergo e2 -elimination.

Q: Problem: Consider the reaction sequence shown below. Pay attention to stereochemistry. (a) Draw the…

A: Ans

Q: Is the following true or false? When you consider the normal polarity of a carbonyl molecule it…

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Q: Br. + NaNH2

A: The objective of the question is to predict the product formed in the given reaction.The reaction…

Q: 14. Explain why pyrrole is an electron-rich heterocycle that is activated toward electrophilic…

A: In case of pyrrole, the l.p. present on N atom is heavily delocalized into the ring to maintain…

Q: a) Propose a mechanism for the following electrophilic aromatic substitution reaction used to make…

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Q: Please don't provide handwritten solution....   Show how the aldol condensation could be used to…

A: In an aldol condensation, the first step is to identify the alpha carbon and the carbonyl group in…

Q: Which of the following is the strongest withdrawing group? methyl bromo amino ketone

A: The inductive effect is a permanent electron displacement of electrons in an organic molecule. The…

Q: Problem: Consider the reaction sequence shown below. Pay attention to stereochemistry. (a) Draw the…

A: Concentrated H3PO4 is a dehydrating agent, and with secondary/tertiary alcohols, form alkenes. With…

Q: The three proton transfer steps result in the intermediate shown below. Draw the curved arrow…

A: To draw the curved arrow mechanism for the following two steps and the products that form, ending…

Q: Decide which compound in pair is more reactive in electrophilic aromatic substitution reaction…

A: In electrophilic substitution reaction benzene reacts acts as nucleophile . So compound which have…

Q: Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and…

A: Bronsted Acid: A species which donates H+ .Bronsted Base:  A accepts which donates H+ .

Q: Draw a mechanism for the reduction of the carboxylic acid with lithium aluminum hydride (LAH).…

A: Lithium aluminum hydride is strong reducing agent. It reduces carboxylic acid to alcohol.

Q: (SYN) Show how to produce each of the following from a hydrocarbon that has the formula indicated. ?…

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Q: a) Draw the mechanism for the reaction of a secondary amine with an acid chloride to make an…

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Q: Is a carbon that is donating its proton a Bronsted acid and Lewis acid , does it also make it an…

A: Introduction: Electrophile and nucleophile: Electrophile means electron loving. Electrophiles are…

Q: Br. + NaNH,

A: The objective of the question is to predict the product formed in the given reaction.The reaction…