Which of the Following Compounds Is the Most Nucleophilic

Answered Sep 12 2016 by Nanin. More questions like this.

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Which of the following compounds is the MOST nucleophilic-CH3OH-BF3-CH3SH-CH3CO2H-H2O.

. Most reactive Least reactive Answer Bank NN-diphenylethanamide acetyl chloride butyl acetate acetic anhydride. Among the given compounds the most susceptible to nucleophilic attack at the carbonyl group is asked Oct 20 2021 in Chemistry by JishaKashyap 611k points class-11. Which of the following is the most polar bond.

See question 2 above D R O O R O. Which of the following compounds is the most reactive in the nucleophilic aromatic substitution reaction with NaOH. O m-nitrochlorobenzene O 35-dinitrochlorobenzene O 24-dinitrochlorobenzene O o-nitrochlorobenzene O p-nitrochlorobenzene.

Correct option is B Aldehydes are generally more reactive than ketones in nucleophilic addition reactions due to steric and electronic reasons. Which of the following compounds is the most nucleophilic. Identify coupling partners that can be used to achieve the following Suzuki coupling.

As discussed above the effectiveness of a leaving group is related to its ability to stabilize a negative charge particularly through having a relatively high electronegativity or. Which of the following factors is favorable for nucleophilicity but not basicity. A mixture of diasteromeric alcohols.

Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution. Benzaldehyde is less reactive than ethanal as the polarity of the carbonyl group is reduced in benzaldehyde due to resonance as shown below. Which of the following compounds is the most reactive in the nucleophilic aromatic substitution reaction with NaOH.

A highly polarizable B low electronegativity. When trans-1-iodo-4-methylcyclohexane is heated in methanol the product mixture is primarily ________. 611 56 List the following bromides in order of their increasing reactivity as substrates in SN2 reactions.

Chemistry questions and answers. PhBr PhCH CH3Br PhCH2Br. A mixture of diasteromeric ethers.

A R NH 2 O B R OCH 3 O C R Cl O Acid chlorides are most reactive. A CH3SH B CH3OH C H2O D CH3CO2H E BF3. 610 49 Rank the species below in order of increasing nucleophilicity in hydroxylic solvents.

Most reactive acetyl chloride acetic anhydride NN-diphenylethanamide butyl acetate Least reactive Answer Bank Incorrect. The steric bulk of t-butoxide decreases its effectiveness as a nucleophile. E following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution.

Which of the following compounds is the most nucleophilic. Which of the following compounds has the least nucleophilic carbon atom. As we all know that the carbonyl compounds undergo nucleophilic addition reaction and this type of reaction are typical of aldehydes and ketones.

B R OCH 3 O. Which of the following compounds is most reactive toward nucleophilic acyl substitution and why. The leaving group ability of the Y group is the most important factor in determining the rate of the second mechanistic step of nucleophilic acyl substitution.

The correct order of reactivity of following compounds in nucleophilic substitution reaction is i CH_3Br ii CH_3Cl Prev Question Next Question 0 votes. Solution for Question 21 Which of the following compounds is the most nucleophilic. Among the given compounds the decreasing order of r4eactivity to nucleophilic attach at carbonyl group is CH_3COClICH_3CHOIICH_3CO OCH_ asked Feb 18 in Chemistry by Anjaliroy 445k points.

See the answer See the answer done loading. If the atom or group is attached with the carbonyl carbon it will decrease the electron density due to negative inductive effect. CI CI CI NO2 O2N NO2 NO2 NO2 NO2 I II III 10 All three are equally reactive towards nucleophilic aromatic substitution.

Which of the following compounds will be the most reactive towards nucleophilic aromatic substitution. CH30- O CH33COH CH3OH O CHCO2-. Ethoxide is the better nucleophile.

H2O CH3CO2- HO- CH3S- Diff. PhBr PhCH2Br and PhCH CH3Br. Click hereto get an answer to your question Which of the following compounds is the most reactive towards nucleophilic acyl substitution.

CH3CO2- CH3S- HO- H2O. O o-nitrochlorobenzene O m-nitrochlorobenzene O 35-dinitrochlorobenzene O 24-dinitrochlorobenzene O p-nitrochlorobenzene. Which of the following compounds has the most nucleophilic carbon atom.

Rank the following compounds from least reactive to most reactive in nucleophilic addition to the carbonyl group with the same nucleophile. Correct option is A Aldehydes are generally more reactive than ketones in nucleophilic addition reaction due to steric and electronic reasons. A CH3SH B CH3OH C H2O D CH3CO2H E BF3.

2-bromo-2-methylpentane 1 - chloro-22-dimethylpentane 1 - chloro - 33 - dimethylpentane bromoethane. Answered Sep 12 2016 by Sleepy. As we are already aware of the fact that addition reactions brought about by a.

Which of the following compounds is the most nucleophilic. Which of the following statements is false regarding the preparation of organolithium compounds. Asked Sep 12 2016 in Chemistry by Carol_P.

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