MgBr

Q: Drawing an Enol and a Ketone Formed by Hydration of an Alkyne Draw the enol intermediate and the…

A: Enol intermediate and the ketone product formed in the reaction:

Q: Draw the product formed when each organometallic reagent is treated with H2O.

A:

Q: What products are formed when each acetal is hydrolyzed with aqueous acid?

A:

Q: Draw the product formed when each organometallic reagent is treated with H2O.

A: (a) Cyclohexane is formed by the abstraction of a proton by cyclohexyllithium from water molecule.…

Q: Draw the products formed from nitration of each compound.

A: (a) Nitration product of p-cresol is, OH group is powerful ortho para directing group than Me so…

Q: Convert each compound to its enol or keto tautomer.

A: Keto-enol tautomerism represents a chemical equilibrium between ketonic and enolic form. Keto and…

Q: Draw the product formed when (CH3)2CHOH is treated with following reagent. H2SO4

A: Alchohol undergoes dehydration in a β-elimination reaction to form an alkene in presence of sulfuric…

Q: Draw the product(s) formed when A is treated with following reagent. LiAlH4, then H2O

A: Given reactant:

Q: Draw the products formed when each compound is treated with HNO3 and H2SO4.State whether the…

A: a) Electron withdrawing groups deactivates the ring towards the electrophilic substitution reaction.…

Q: Draw the product formed when pentanal (CH3CH2CH2CH2CHO) is treatedwith following reagent. With some…

A: Pentanal when treated with the given reagent (CH3MgBr, H2O) results in the formation of 2-hexanol

Q: Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent.…

A:

Q: Draw the six products (including stereoisomers) formed when A is treated with NBS + hv.

A:

Q: Draw the product formed when each compound is treated with two equivalents of CH3CH2CH2CH2MgBr…

A: The given compounds contain the carbonyl groups. The reagent given is an organometallic compound.…

Q: Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent.…

A: Given, CH3COCl

Q: Draw the products formed in each reaction sequence.

A: Introduction: Witting reaction: It is an organic reaction in which a triphenylphosphonium ylide…

Q: Draw the products formed when each compound is treated with HNO3 and H2SO4.

A: -OCH3 is ortho, para director whereas -COOCH3 is a meta director. Because -OCH3 is a strong…

Q: Draw the products formed when each compound is treated with one equivalent of HBr.

A: The products are as drawn below:

Q: Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent.…

A: The reactant is p-methylaniline. It contains a methyl and an amino group. The -NH2 group is basic in…

Q: Draw the products formed when each naturally occurring compound is treated with O3 followed by Zn,…

A:

Q: Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent.…

A: The nitration of primary aromatic amines with nitrous acid (generated in situ from sodium nitrite…

Q: a. CHO b.

A: Intermolecular aldol reaction leads to the formation of unsaturated carbonyl compound. In…

Q: Explain this

A: Nitration indicates the adding of -NO2 group. Mononitration of a benzene ring results in the…

Q: Ioos со СН3 СН3

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Draw enol tautomer(s) for each compound.

A:

Q: Draw the products formed in each reaction sequence.

A:

Q: Draw the enol or keto tautomer(s) of each compound.

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: Draw the products formed when each acetal is treated with aqueous acid.

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: What products are formed when each acetal is hydrolyzed with aqueous acid?

A: The reaction of an alcohol with aldehyde and ketone in the presence of acid produces acetal or…

Q: Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with each reagent. With some…

A: Reaction of carboxylic acid with NaHCO3 liberates CO2.

Q: Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. HCl

A: The molecular formula of p-methyl aniline – (p-CH3C6H4NH2)

Q: а. NaBHa, CH3ОН b. [1] LIAIH4; [2] H2O с. [1] CН:MgBr; [2] H-0 d. HOCH:CH20Н, Н" е. NaCN, HCI

A:

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.