Which of the following undergoes nucleophilic substitution exclusively by `S_(N^(1))` mechanism?

Which of the following undergoes nucleophilic substitution exclusively by `S_(N^(1))` mechanism?
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Which of the following undergoes nucleophilic substitution exclusively by `S_(N^(1))` ... Isopropyl chloride C. Chlorobenzene D. Benzyl chloride
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Quinoline undergoes nucleophilic substitution on heating with NaNH2 to give (a) 2-Aminoquinoline (b) 4-Aminoquinoline (c) 3-Aminoquinoline (d) 8-Aminoquinoline

Description : Quinoline undergoes nucleophilic substitution on heating with NaNH2 to give (a) 2-Aminoquinoline (b) 4-Aminoquinoline (c) 3-Aminoquinoline (d) 8-Aminoquinoline

Last Answer : 2-Aminoquinoline

Acetyl chloride undergoes nucleophilic substitution at a faster rate than methyl acetate because __________. (a) the ester is more sterically hindered than the acid chloride (b) the acid chloride is more sterically hindered than the ester (c) the methoxide is a better leaving group than chloride (d) chloride is a better leaving group than methoxide

Description : Acetyl chloride undergoes nucleophilic substitution at a faster rate than methyl acetate because __________. (a) the ester is more sterically hindered than the acid chloride (b) the acid chloride is ... is a better leaving group than chloride (d) chloride is a better leaving group than methoxide

Last Answer : chloride is a better leaving group than methoxide

Which of the following can undergo nucleophilic substitution under ordinary conditions? I Allyl chloride II Benzyl chloride III n-Propyl chloride IV V

Description : Which of the following can undergo nucleophilic substitution under ordinary conditions? I Allyl chloride II Benzyl chloride III n-Propyl chloride IV V

Last Answer : Which of the following can undergo nucleophilic substitution under ordinary conditions? I Allyl chloride II ... are correct D. I and III are correct

In a `S_(N^(2))` substitution reaction of the type `R-Br+Cl^(-)overset("DMF")rarrR-Cl+Br^(-)` Which one of the following has the highest relative rate

Description : In a `S_(N^(2))` substitution reaction of the type `R-Br+Cl^(-)overset("DMF")rarrR-Cl+Br^(-)` Which one of the following has the highest relative rate

Last Answer : In a `S_(N^(2))` substitution reaction of the type `R-Br+Cl^(-)overset("DMF")rarrR-Cl+Br^(-)` Which one of ... CH_(2)Br` D. `(CH_(3))_(2)CH-CH_(2)Br`

KI in acetone, undergoes `S_(N)2` reaction with each of `P,Q ,R` and S The rates of the reaction very as `underset(P)(H_(3)C-Cl)` .

Description : KI in acetone, undergoes `S_(N)2` reaction with each of `P,Q ,R` and S The rates of the reaction very as `underset(P)(H_(3)C-Cl)` .

Last Answer : KI in acetone, undergoes `S_(N)2` reaction with each of `P,Q ,R` and S The rates of the reaction very as ` ... R gt Q gt S D. R gt P gt S gt Q

An organic compound (A) has a molecular weight 78 and an empirical formula CH. (A) is resistant to attack by oxidizing agents but undergoes substitution and addition reactions. X-ray analysis shows that the distance between adjacent carbon atoms is 1.39Å (intermediate between single and double bond lengths). The evidence suggests that compound (A) is (a) Benzene (b) Cyclohexane (c) Toluene (d) n-Hexane

Description : An organic compound (A) has a molecular weight 78 and an empirical formula CH. (A) is resistant to attack by oxidizing agents but undergoes substitution and addition reactions. X-ray analysis shows that the ... suggests that compound (A) is (a) Benzene (b) Cyclohexane (c) Toluene (d) n-Hexane

Last Answer : Benzene

An organic compound (A) has a molecular weight 78 and an empirical formula CH. (A) is resistant to attack by oxidizing agents but undergoes substitution and addition reactions. X-ray analysis shows that the distance between adjacent carbon atoms is 1.39Å (intermediate between single and double bond lengths). The evidence suggests that compound (A) is (a) Benzene (b) Cyclohexane (c) Toluene (d) n-Hexane

Description : An organic compound (A) has a molecular weight 78 and an empirical formula CH. (A) is resistant to attack by oxidizing agents but undergoes substitution and addition reactions. X-ray analysis shows that the ... suggests that compound (A) is (a) Benzene (b) Cyclohexane (c) Toluene (d) n-Hexane

Last Answer : Benzene

Explain why nucleophilic substitution reactions are not very common in phenols.

Description : Explain why nucleophilic substitution reactions are not very common in phenols.

Last Answer : Explain why nucleophilic substitution reactions are not very common in phenols.

(A) Ethyl chloride is more reactive than vinyl chloride towards nucleophilic substitution reactions. (R) Vinyl chloride is `+I` electron pushing group

Description : (A) Ethyl chloride is more reactive than vinyl chloride towards nucleophilic substitution reactions. (R) Vinyl chloride is `+I` electron pushing group

Last Answer : (A) Ethyl chloride is more reactive than vinyl chloride towards nucleophilic substitution reactions. (R) Vinyl ... A) is incorrect but (R) is correct.

Which one of the following is most reactive towards nucleophilic substitution reaction ?

Description : Which one of the following is most reactive towards nucleophilic substitution reaction ?

Last Answer : Which one of the following is most reactive towards nucleophilic substitution reaction ? A. `H_(2)C=CH-Cl` B. ` ... 3)CH=CHCl` D. `ClCH_(2)-CH=CH_(2)`

Which of the following is least reactive in a nucleophilic substitution reaction?

Description : Which of the following is least reactive in a nucleophilic substitution reaction?

Last Answer : Which of the following is least reactive in a nucleophilic substitution reaction? A. `(CH_(3))_(3)C-Cl` B. `CH_ ... 3)CH_(2)Cl` D. `CH_(2)=CHCH_(2)Cl`

Why does benzene undergo electrophilic substitution reactions easily and nucleophilic substitutions with difficulty?

Description : Why does benzene undergo electrophilic substitution reactions easily and nucleophilic substitutions with difficulty?

Last Answer : Ans. Due to the presence of an electron cloud containing 6 pi electrons above and below the plane of the ring, benzene is a source of electrons. Consequently, it attracts ... . As a result, benzene undergoes electrophilic substitution reactions easily and nucleophilic substitution with difficulty.

Aryl halides are less reactive towards nucleophilic substitution as compared to alkyl halides due to (a) Inductive effect (b) Resonance stabilization (c) Tautomerism (d) Stereoisomerism

Description : Aryl halides are less reactive towards nucleophilic substitution as compared to alkyl halides due to (a) Inductive effect (b) Resonance stabilization (c) Tautomerism (d) Stereoisomerism

Last Answer : Resonance stabilization

Benzene reacts with concentrated HNO3 in the presence of concentrated H2SO4 to give nitrobenzene. This reaction is an example of (a) Electrophilic addition (b) Nucleophilic addition (c) Electrophilic substitution (d) Nucleophilic substitution

Description : Benzene reacts with concentrated HNO3 in the presence of concentrated H2SO4 to give nitrobenzene. This reaction is an example of (a) Electrophilic addition (b) Nucleophilic addition (c) Electrophilic substitution (d) Nucleophilic substitution

Last Answer : Electrophilic substitution

Benzene reacts with concentrated HNO3 in the presence of concentrated H2SO4 to give nitrobenzene. This reaction is an example of (a) Electrophilic addition (b) Nucleophilic addition (c) Electrophilic substitution (d) Nucleophilic substitution

Description : Benzene reacts with concentrated HNO3 in the presence of concentrated H2SO4 to give nitrobenzene. This reaction is an example of (a) Electrophilic addition (b) Nucleophilic addition (c) Electrophilic substitution (d) Nucleophilic substitution

Last Answer : Electrophilic substitution

Esters can be formed by nucleophilic substitution reactions of : (a) carboxylic acids and alcohols ; acid-catalyzed (b) acid chlorides and alcohols (c) both of the above (d) neither of the above

Description : Esters can be formed by nucleophilic substitution reactions of : (a) carboxylic acids and alcohols ; acid-catalyzed (b) acid chlorides and alcohols (c) both of the above (d) neither of the above

Last Answer : both of the above

Esters and amides are most easily made by nucleophilic acyl substitution reactions on : (a) acid anhydrides (b) carboxylates (c) carboxylic acids (d) acid chlorides

Description : Esters and amides are most easily made by nucleophilic acyl substitution reactions on : (a) acid anhydrides (b) carboxylates (c) carboxylic acids (d) acid chlorides

Last Answer : acid chlorides

The characteristic reaction of carboxylic acids is : (a) electrophilic addition (b) electrophilic substitution (c) nucleophilic addition (d) nucleophilic substitution

Description : The characteristic reaction of carboxylic acids is : (a) electrophilic addition (b) electrophilic substitution (c) nucleophilic addition (d) nucleophilic substitution

Last Answer : nucleophilic substitution

Why do aldehydes undergo nucleophilic addition reactions while esters undergo nucleophilic acyl substitution reactions? (a) The carbonyl carbon of an ester is more electrophilic than that of an aldehyde. (b) Aldehydes are more sterically hindered than esters. (c) Once the nucleophile adds to an aldehyde, the tetrahedral intermediate is too sterically hindered to eliminate one of the attached groups. (d) Once the nucleophile adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic

Description : Why do aldehydes undergo nucleophilic addition reactions while esters undergo nucleophilic acyl substitution reactions? (a) The carbonyl carbon of an ester is more electrophilic than that of an aldehyde. (b) ... adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic

Last Answer : Once the nucleophile adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic

Which of the following characterizes the reactions of aldehydes and ketones? (a) electrophilic addition (b) electrophilic substitution (c) nucleophilic acyl substitution (d) nucleophilic addition; free radical addition

Description : Which of the following characterizes the reactions of aldehydes and ketones? (a) electrophilic addition (b) electrophilic substitution (c) nucleophilic acyl substitution (d) nucleophilic addition; free radical addition

Last Answer : nucleophilic addition; free radical addition

Acetone reacts with HCN to form a cyanohydrin. It is an example of (a) Electrophilic addition (b) Electrophilic substitution (c) Nucleophilic addition(d) Nucleophilic substitution

Description : Acetone reacts with HCN to form a cyanohydrin. It is an example of (a) Electrophilic addition (b) Electrophilic substitution (c) Nucleophilic addition (d) Nucleophilic substitution

Last Answer : Nucleophilic addition

Which alkyl halides react most readily by nucleophilic substitution? (a) CH3CH2Cl (b) CH3CH2I (c) CH3CH2Br (d) CH3CH2F

Description : Which alkyl halides react most readily by nucleophilic substitution? (a) CH3CH2Cl (b) CH3CH2I (c) CH3CH2Br (d) CH3CH2F

Last Answer : CH3CH2I

Alkyl halides undergo (a) Electrophilic substitution reactions (b) Electrophilic addition reactions (c) Nucleophilic substitution reactions (d) Nucleophilic addition reactions

Description : Alkyl halides undergo (a) Electrophilic substitution reactions (b) Electrophilic addition reactions (c) Nucleophilic substitution reactions (d) Nucleophilic addition reactions

Last Answer : Nucleophilic substitution reactions

Propene reacts with bromine to form 1,2-dibromopropane. This is an example of (a) Nucleophilic addition (b) Electrophilic addition (c) Nucleophilic substitution (d) Electrophilic substitution

Description : Propene reacts with bromine to form 1,2-dibromopropane. This is an example of (a) Nucleophilic addition (b) Electrophilic addition (c) Nucleophilic substitution (d) Electrophilic substitution

Last Answer : Electrophilic addition

Ethylene is obtained from ethyl bromide by : (a) Simple heating (b) Hydrolysis (c) Dehydrohalogenation (d) Nucleophilic substitution

Description : Ethylene is obtained from ethyl bromide by : (a) Simple heating (b) Hydrolysis (c) Dehydrohalogenation (d) Nucleophilic substitution

Last Answer : Dehydrohalogenation

The chlorination of methane to give CCl4 is an example of (a) an electrophilic addition (b) a free-radical substitution (c) a nucleophilic addition (d) an electrophilic substitution

Description : The chlorination of methane to give CCl4 is an example of (a) an electrophilic addition (b) a free-radical substitution (c) a nucleophilic addition (d) an electrophilic substitution

Last Answer : a free-radical substitution

The hydrolysis of 2-bromo-3-methylbutane by `S_(N^(1))` mechanism gives meinly:

Description : The hydrolysis of 2-bromo-3-methylbutane by `S_(N^(1))` mechanism gives meinly:

Last Answer : The hydrolysis of 2-bromo-3-methylbutane by `S_(N^(1))` mechanism gives meinly: A. 3-methyl-2- ... . 2,2-dimethyl-2-propanol D. 2-methyl-1-butanol

Which one of the following halogen compounds is difficult to be hydrolysed by `S_(N^(1))` mechanism?

Description : Which one of the following halogen compounds is difficult to be hydrolysed by `S_(N^(1))` mechanism?

Last Answer : Which one of the following halogen compounds is difficult to be hydrolysed by `S_(N^(1)) ... B. Isopropyl chloride C. Benzyl chloride D. Chlorobenzene

The compound that does not undergo hydrolysis by `S_(N^(1))` mechanism is :

Description : The compound that does not undergo hydrolysis by `S_(N^(1))` mechanism is :

Last Answer : The compound that does not undergo hydrolysis by `S_(N^(1))` mechanism is : A. `H_(2)C=CHCH_(2)Cl` B. `C_(6) ... )Cl` D. `C_(6)H_(5)CH(C_(6)H_(5))Cl`

Which of the following alkyl halides is hydrolysed by `S_(N^(1))` mechanism?

Description : Which of the following alkyl halides is hydrolysed by `S_(N^(1))` mechanism?

Last Answer : Which of the following alkyl halides is hydrolysed by `S_(N^(1))` mechanism? A. `CH_(3)Cl` B. `CH_(3)CH_(2)Cl` ... (2)CH_(2)Cl` D. `(CH_(3))_(3)"CCl"`

`S_(N^(1))` mechanism for the hydrolysis of an alkyl halide involves the formation of intermediate:

Description : `S_(N^(1))` mechanism for the hydrolysis of an alkyl halide involves the formation of intermediate:

Last Answer : `S_(N^(1))` mechanism for the hydrolysis of an alkyl halide involves the formation of intermediate: ... B. carbocation C. carbanion D. none of these

Which of the following statements describes the first step in the mechanism of the aldol condensation? (a) An alpha hydrogen is abstracted by the base to form an enolate anion. (b) A nucleophilic base attacks the carbonyl carbon atom. (c) The carbonyl oxygen is protonated by the base ion. (d) The alpha hydrogen is abstracted by an acid to the enolate anion.

Description : Which of the following statements describes the first step in the mechanism of the aldol condensation? (a) An alpha hydrogen is abstracted by the base to form an enolate anion. (b) A nucleophilic base attacks ... by the base ion. (d) The alpha hydrogen is abstracted by an acid to the enolate anion.

Last Answer : An alpha hydrogen is abstracted by the base to form an enolate anion

Which of the following compounds undergoes mucleophilic substitution reaction most easily?

Description : Which of the following compounds undergoes mucleophilic substitution reaction most easily?

Last Answer : Which of the following compounds undergoes mucleophilic substitution reaction most easily? A. B. C. D.

Pyridine undergoes nuclophilic substitution with NaNH2 at 100°C to form (a) 2-Aminopyridine (b) 3-Aminopyridine (c) 4-Aminopyridine (d) None of these

Description : Pyridine undergoes nuclophilic substitution with NaNH2 at 100°C to form (a) 2-Aminopyridine (b) 3-Aminopyridine (c) 4-Aminopyridine (d) None of these

Last Answer : 2-Aminopyridine

Pyridine undergoes electrophilic substitution with fuming H2SO4 at 350°C to give (a) 2-Pyridinesulfonic acid (b) 4-Pyridinesulfonic acid (c) 3-Pyridinesulfonic acid (d) None of these

Description : Pyridine undergoes electrophilic substitution with fuming H2SO4 at 350°C to give (a) 2-Pyridinesulfonic acid (b) 4-Pyridinesulfonic acid (c) 3-Pyridinesulfonic acid (d) None of these

Last Answer : 3-Pyridinesulfonic acid

Anthracene undergoes electrophilic substitution reactions mainly at (a) C-1 (b) C-2 (c) C-9 (d) C-1 and C-2

Description : Anthracene undergoes electrophilic substitution reactions mainly at (a) C-1 (b) C-2 (c) C-9 (d) C-1 and C-2

Last Answer : C-9

Benzene undergoes substitution reaction more easily than addition reaction because (a) it has a cyclic structure (b) it has three double bonds (c) it has six hydrogen atoms (d) there is delocalization of electrons

Description : Benzene undergoes substitution reaction more easily than addition reaction because (a) it has a cyclic structure (b) it has three double bonds (c) it has six hydrogen atoms (d) there is delocalization of electrons

Last Answer : there is delocalization of electrons

Benzene undergoes substitution reaction more easily than addition reaction because (a) it has a cyclic structure (b) it has three double bonds (c) it has six hydrogen atoms (d) there is delocalization of electrons

Description : Benzene undergoes substitution reaction more easily than addition reaction because (a) it has a cyclic structure (b) it has three double bonds (c) it has six hydrogen atoms (d) there is delocalization of electrons

Last Answer : there is delocalization of electrons

Which of the reactions between the following pairs of reagents proceeds by a mechanism that may be described as an electrophilic substitution? (a) Benzene + Br2/FeBr3 (b) Propene + Br2 (c) Acetone + NH2NH2 (d) Ethyl bromide + aq KOH

Description : Which of the reactions between the following pairs of reagents proceeds by a mechanism that may be described as an electrophilic substitution? (a) Benzene + Br2/FeBr3 (b) Propene + Br2 (c) Acetone + NH2NH2 (d) Ethyl bromide + aq KOH

Last Answer : Benzene + Br2/FeBr3

Which of the following is not a correct statement about the electrophilic substitution mechanism of benzene? (a) Benzene functions as a nucleophile. (b) Formation of a carbocation intermediate is the rate-determining step. (c) The carbocation intermediate contains an sp3 hybridized carbon in the ring. (d) The addition product is a frequently observed minor product.

Description : Which of the following is not a correct statement about the electrophilic substitution mechanism of benzene? (a) Benzene functions as a nucleophile. (b) Formation of a carbocation intermediate is the ... hybridized carbon in the ring. (d) The addition product is a frequently observed minor product.

Last Answer : The addition product is a frequently observed minor product.

Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

Description : Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

Last Answer : Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

Description : Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

Last Answer : Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

If `alpha, beta` are roots of equation `x^(2)-4x-3=0` and `s_(n)=alpha^(n)+beta^(n), n in N` then the value of `(s_(7)-4s_(6))/s_(5)` is

Description : If `alpha, beta` are roots of equation `x^(2)-4x-3=0` and `s_(n)=alpha^(n)+beta^(n), n in N` then the value of `(s_(7)-4s_(6))/s_(5)` is

Last Answer : If `alpha, beta` are roots of equation `x^(2)-4x-3=0` and `s_(n)=alpha^(n)+beta^(n), n in N` then the value ... 4s_(6))/s_(5)` is A. 4 B. 3 C. 5 D. 7

Some amount of "20V" `H_(2)O_(2)` is mixed with excess of acidified solution of Kl. The iodine so liberated required 200 mL of 0.1 N `Na_(2)S_(2)O_(3)

Description : Some amount of "20V" `H_(2)O_(2)` is mixed with excess of acidified solution of Kl. The iodine so liberated required 200 mL of 0.1 N `Na_(2)S_(2)O_(3)

Last Answer : Some amount of "20V" `H_(2)O_(2)` is mixed with excess of acidified solution of Kl. The iodine so liberated ... 56 mL B. 112 mL C. 168 mL D. 224 mL

Some amount of "20V" `H_(2)O_(2)` is mixed with excess of acidified solution of Kl. The iodine so liberated required 200 mL of 0.1 N `Na_(2)S_(2)O_(3)

Description : Some amount of "20V" `H_(2)O_(2)` is mixed with excess of acidified solution of Kl. The iodine so liberated required 200 mL of 0.1 N `Na_(2)S_(2)O_(3)

Last Answer : Some amount of "20V" `H_(2)O_(2)` is mixed with excess of acidified solution of Kl. The iodine so liberated required ... . 0.8 g C. 4.2 g D. 0.98 g

Some amount of "20V" `H_(2)O_(2)` is mixed with excess of acidified solution of Kl. The iodine so liberated required 200 mL of 0.1 N `Na_(2)S_(2)O_(3)

Description : Some amount of "20V" `H_(2)O_(2)` is mixed with excess of acidified solution of Kl. The iodine so liberated required 200 mL of 0.1 N `Na_(2)S_(2)O_(3)

Last Answer : Some amount of "20V" `H_(2)O_(2)` is mixed with excess of acidified solution of Kl. The iodine so liberated required ... 37.2 mL C. 5.6 mL D. 22.4 mL

`underset("Brown")([(NH_(3))_(5)Co-O-O-Co(NH_(3))_(5)]^(4+)) underset("oxidise")overset([S_(2)O_(8)]^(2-))tounderset("Green")([(NH_(3))_(5)Co-O-O-Co(N

Description : `underset("Brown")([(NH_(3))_(5)Co-O-O-Co(NH_(3))_(5)]^(4+)) underset("oxidise")overset([S_(2)O_(8)]^(2-))tounderset("Green")([(NH_(3))_(5)Co-O-O-Co(N

Last Answer : `underset("Brown")([(NH_(3))_(5)Co-O-O-Co(NH_(3))_(5)]^(4+)) underset("oxidise")overset([S_(2)O_(8) ... III " "IV" & "III" "III),("brown "" green"):}`

(A) In `S_(N^(2))` reactions, complete inversion of configuration takes place. (R) In `S_(N^(1))` reactions, retention but not the inversion takes pla

Description : (A) In `S_(N^(2))` reactions, complete inversion of configuration takes place. (R) In `S_(N^(1))` reactions, retention but not the inversion takes pla

Last Answer : (A) In `S_(N^(2))` reactions, complete inversion of configuration takes place. (R) In `S_(N^(1))` ... . D. IF (A) is incorrect but (R) is correct.

(A) `S_(N^(2))` reactioin takes place in single step. (R) `S_(N^(2))` reaction involves transition state intermediate.

Description : (A) `S_(N^(2))` reactioin takes place in single step. (R) `S_(N^(2))` reaction involves transition state intermediate.

Last Answer : (A) `S_(N^(2))` reactioin takes place in single step. (R) `S_(N^(2))` reaction involves transition ... . D. IF (A) is incorrect but (R) is correct.

Which is/are correctly linked here? `{:(,"List I",,"List II"),((a),E_(1)Cb,(a),"Carbanion formation"),((b),E_(2),(b),"Stereo specific"),((c),S_(N^(1))

Description : Which is/are correctly linked here? `{:(,"List I",,"List II"),((a),E_(1)Cb,(a),"Carbanion formation"),((b),E_(2),(b),"Stereo specific"),((c),S_(N^(1))

Last Answer : Which is/are correctly linked here? `{:(,"List I",,"List II"),((a),E_(1)Cb,(a),"Carbanion formation" ... "),((d),E_(1),(d),"Carbocation formation"):}`