Which of the following halides will be most reactive towards `S_(N^(2))` reaction?

Which of the following halides will be most reactive towards `S_(N^(2))` reaction?
by

1 Answer

Answer :

Which of the following halides will be most reactive towards `S_(N^(2))` reaction? A. `C_(6)H_(5)CH_(2 ... (2)-underset(Br)underset("| ")"CH"-CH_(3)`
by
selected by

Related questions

Which one is most reactive towards `S_(N^(1))` reaction?

Description : Which one is most reactive towards `S_(N^(1))` reaction?

Last Answer : Which one is most reactive towards `S_(N^(1))` reaction? A. `C_(6)H_(5)CH(C_(6)H_(5))Br` B. `C_(6)H_(5) ... H_(5)CH(CH_(3))Br` D. `C_(6)H_(5)CH_(2)Br`

The correct increasing order of the reactivity of halides for `S_(N^(1))` reaction is:

Description : The correct increasing order of the reactivity of halides for `S_(N^(1))` reaction is:

Last Answer : The correct increasing order of the reactivity of halides for `S_(N^(1))` reaction is: A. `CH_(3)CH_(2)-Xlt( ... -Xlt(CH_(3))_(2)CH-XltCH_(3)CH_(2)-X`

The order of reactivities of the following alkyl halides for a `S_(N^(2))` reaction is :

Description : The order of reactivities of the following alkyl halides for a `S_(N^(2))` reaction is :

Last Answer : The order of reactivities of the following alkyl halides for a `S_(N^(2))` reaction is : A. RF > RCl > RBr > ... RBr > RF > RI D. RI > RBr > RCl > RF

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

The `S_(N^(1))` reactivity of the following halides will be in the order: (i) `(CH_(3))_(3)C-Br` (ii) `(C_(6)H_(5))CHBr` (iii) `(C_(6)H_(5))_(2)C(CH_(

Description : The `S_(N^(1))` reactivity of the following halides will be in the order: (i) `(CH_(3))_(3)C-Br` (ii) `(C_(6)H_(5))CHBr` (iii) `(C_(6)H_(5))_(2)C(CH_(

Last Answer : The `S_(N^(1))` reactivity of the following halides will be in the order: (i) `(CH_(3))_(3)C-Br` (ii) `(C_ ... D. (iii) gt (ii) gt (i) gt (iv) gt (v)

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"`

Which of the following halides is least reactive in an E2 reaction with sodium methoxide? (a) (CH3)3CCH2I (b) (CH3)2CHCHICH3 (c) (CH3)2CHCH2Br (d) (CH3)2CHCH2Cl

Description : Which of the following halides is least reactive in an E2 reaction with sodium methoxide? (a) (CH3)3CCH2I (b) (CH3)2CHCHICH3 (c) (CH3)2CHCH2Br (d) (CH3)2CHCH2Cl

Last Answer : (CH3)3CCH2I

Which of the following halides is most reactive in an E2 reaction with sodium methoxide? (a) (CH3)3CCH2I (b) (CH3)2CHCHICH3 (c) (CH3)2CHCH2Br (d) (CH3)2CHCH2C

Description : Which of the following halides is most reactive in an E2 reaction with sodium methoxide? (a) (CH3)3CCH2I (b) (CH3)2CHCHICH3 (c) (CH3)2CHCH2Br (d) (CH3)2CHCH2C

Last Answer : (CH3)2CHCHICH3

Arrange the following in order of decreasing tendency towards `S_(N^(2))` reaction : `{:(underset("(I)")(CH_(3)CH_(2)CH_(2)CH_(2)Cl)", "underset("(II)

Description : Arrange the following in order of decreasing tendency towards `S_(N^(2))` reaction : `{:(underset("(I)")(CH_(3)CH_(2)CH_(2)CH_(2)Cl)", "underset("(II)

Last Answer : Arrange the following in order of decreasing tendency towards `S_(N^(2))` reaction : `{: ... `IIIgtIVgtIIgtI` C. `IgtIIIgtIIgtIV` D. `IIgtIgtIIIgtIV`

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)`

Phenol is more reactive than benzene towards electrophilic substitution reaction. In case of Phenol, the intermediate carbocation is more resonance st

Description : Phenol is more reactive than benzene towards electrophilic substitution reaction. In case of Phenol, the intermediate carbocation is more resonance st

Last Answer : Phenol is more reactive than benzene towards electrophilic substitution reaction. In case of Phenol, the ... D. A is incorrect but R is correct

Which of the following halogen acids is most reactive towards the given reaction ? `R-O-R overset(HX)rarr`

Description : Which of the following halogen acids is most reactive towards the given reaction ? `R-O-R overset(HX)rarr`

Last Answer : Which of the following halogen acids is most reactive towards the given reaction ? `R-O-R overset(HX)rarr` A. HCl B. HI C. HBr D. Equally reactive

(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 of the following are correct for `S_(N^(2))` reaction?

Description : Which of the following are correct for `S_(N^(2))` reaction?

Last Answer : Which of the following are correct for `S_(N^(2))` reaction? A. The reaction intermediate ... solvents D. It is favoured by stability of carbocation

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

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`

In the `S_(N^(1))` reaction on chiral centres there is :

Description : In the `S_(N^(1))` reaction on chiral centres there is :

Last Answer : In the `S_(N^(1))` reaction on chiral centres there is : A. `100%` racemization B. ... partial racemization C. `100%` retention D. `100%` inversion

As `S_(N^(2))` reaction at an asymmetric carbon of a compound always gives:

Description : As `S_(N^(2))` reaction at an asymmetric carbon of a compound always gives:

Last Answer : As `S_(N^(2))` reaction at an asymmetric carbon of a compound always gives: A. an ... C. a mixture of diastereomers D. a single stereoisomer

Which of the following reactions is an example of `S_(N^(2))` reaction?

Description : Which of the following reactions is an example of `S_(N^(2))` reaction?

Last Answer : Which of the following reactions is an example of `S_(N^(2))` reaction? A. `(CH_(3))_(3)C-Br+OH^(-) ... )CH_(2)OHunderset((-H_(2)O))rarrH_(2)C=CH_(2)`

Which one of the following statements wrong about `S_(N^(2))` reaction?

Description : Which one of the following statements wrong about `S_(N^(2))` reaction?

Last Answer : Which one of the following statements wrong about `S_(N^(2))` reaction? A. The rate of ... The rate of reaction `prop` [substrate] [nucleophile]

Number of halides undergoing complete reaction in presence of water under normal conditions is : (i) `BF_(3)` (ii) `BCl_(3)` (iii) `NCl_(3)` (iv) `AlC

Description : Number of halides undergoing complete reaction in presence of water under normal conditions is : (i) `BF_(3)` (ii) `BCl_(3)` (iii) `NCl_(3)` (iv) `AlC

Last Answer : Number of halides undergoing complete reaction in presence of water under normal conditions is : (i) `BF_(3)` (ii ... (vi) `PCl_(3)` (vii) `AsCl_(3)`

Number of halides undergoing complete reaction in presence of water under normal conditions is : (i) `BF_(3)` (ii) `BCl_(3)` (iii) `NCl_(3)` (iv) `AlC

Description : Number of halides undergoing complete reaction in presence of water under normal conditions is : (i) `BF_(3)` (ii) `BCl_(3)` (iii) `NCl_(3)` (iv) `AlC

Last Answer : Number of halides undergoing complete reaction in presence of water under normal conditions is : (i) `BF_(3)` (ii ... (vi) `PCl_(3)` (vii) `AsCl_(3)`

Grignard reagents do not show any reaction with (a) Alkoxyalkanes (b) Alkanones (c) Alkyl alkanoates (d) Acyl halides

Description : Grignard reagents do not show any reaction with (a) Alkoxyalkanes (b) Alkanones (c) Alkyl alkanoates (d) Acyl halides

Last Answer : Alkoxyalkanes

Which of the following statements concerning SN2 reactions of alkyl halides is not correct? (a) The rate of reaction depends on the concentration of the nucleophile. (b) The rate of reaction depends on the concentration of the alkyl halide. (c) The rate of reaction of a particular alkyl bromide depends on the steric accessibility of the carbon of the C-Br bond. (d) All alkyl iodides react more rapidly than all alkyl chlorides

Description : Which of the following statements concerning SN2 reactions of alkyl halides is not correct? (a) The rate of reaction depends on the concentration of the nucleophile. (b) The rate of reaction depends on the ... carbon of the C-Br bond. (d) All alkyl iodides react more rapidly than all alkyl chlorides

Last Answer : All alkyl iodides react more rapidly than all alkyl chlorides

Statement I: In strongly acidic solutions , anline becomes more reactive towards electrophilic reagents Statement II: The amino group being completely

Description : Statement I: In strongly acidic solutions , anline becomes more reactive towards electrophilic reagents Statement II: The amino group being completely

Last Answer : Statement I: In strongly acidic solutions , anline becomes more reactive towards electrophilic reagents ... Assertion is false but Reason is true.

(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 electrophilic attack?

Description : Which one of the following is most reactive towards electrophilic attack?

Last Answer : Which one of the following is most reactive towards electrophilic attack? A. B. C. D.

Assertion: Phenol is more reactive than benzene towards electrophilic reactions. Reason : The +R effect of OH group increases the electron density on

Description : Assertion: Phenol is more reactive than benzene towards electrophilic reactions. Reason : The +R effect of OH group increases the electron density on

Last Answer : Assertion: Phenol is more reactive than benzene towards electrophilic reactions. Reason : The +R effect of ... D. A is incorrect but R is correct

Which alcohol is most reactive towards `HCl` in the presence of anhydrous `ZnCl_(2)`?

Description : Which alcohol is most reactive towards `HCl` in the presence of anhydrous `ZnCl_(2)`?

Last Answer : Which alcohol is most reactive towards `HCl` in the presence of anhydrous `ZnCl_(2)`? A. primary B. secondary C. tertiary D. all of these

40. Among the fo the one that is most reactive towards electrophilic nitration is: (1) Benzene (2) Benzoic acid (3) Nitrobenzene (4) Toluene

Description : 40. Among the following compounds the one that is most reactive towards electrophilic nitration is: (1) Benzene (2) Benzoic acid (3) Nitrobenzene (4) Toluene

Last Answer : Toluene

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.

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"):}`

The most easily hydrolysed molecule under `S_(N^(1))` condition is:

Description : The most easily hydrolysed molecule under `S_(N^(1))` condition is:

Last Answer : The most easily hydrolysed molecule under `S_(N^(1))` condition is: A. allyl chloride B. benzyl chloride C. ethyl chloride D. isopropyl chloride

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 of the following is the correct order of decreasing `S_(N^(2))` reactivity ?

Description : Which of the following is the correct order of decreasing `S_(N^(2))` reactivity ?

Last Answer : Which of the following is the correct order of decreasing `S_(N^(2))` reactivity ? A. `R_(2)CHXgtR_(3) ... 3)CXgtR_(2)CHXgtRCH_(2)X("X is a halogen")`

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

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

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

Last Answer : Which of the following undergoes nucleophilic substitution exclusively by `S_(N^(1))` ... Isopropyl chloride C. Chlorobenzene D. Benzyl chloride

Consider the following bromides: The correct order of `S_(N^(1))` reactivity is :

Description : Consider the following bromides: The correct order of `S_(N^(1))` reactivity is :

Last Answer : Consider the following bromides: The correct order of `S_(N^(1))` reactivity is : A. `IgtIIgtIII` B. `IIgtIIIgtI` C. `IIgtIgtIII` D. `IIIgtIIgtI`

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`

`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

`n(CF_(2)=CF_(2))overset((NH_(4))_(2)S_(2)O_(8))underset(Heat)toX` Here , X is:

Description : `n(CF_(2)=CF_(2))overset((NH_(4))_(2)S_(2)O_(8))underset(Heat)toX` Here , X is:

Last Answer : `n(CF_(2)=CF_(2))overset((NH_(4))_(2)S_(2)O_(8))underset(Heat)toX` Here , X is: A. PVC B. PMMA C. PAN D. none of these

Asseration: Number of `S-S` bonds in `H_(2)S_(n)O_(6)` is (n-1). Reason: `H_(2)S_(n)O_(6)` shows `HO_(3)S-underset((n-2))(S)-SO_(3)H`

Description : Asseration: Number of `S-S` bonds in `H_(2)S_(n)O_(6)` is (n-1). Reason: `H_(2)S_(n)O_(6)` shows `HO_(3)S-underset((n-2))(S)-SO_(3)H`

Last Answer : Asseration: Number of `S-S` bonds in `H_(2)S_(n)O_(6)` is (n-1). Reason: `H_(2)S_(n)O_(6)` shows `HO_(3)S-underset((n-2))(S)-SO_(3)H`

`S_(1):(HPO_(3))_(n)` can be prepared by heating phosphorous acid and bromine in a sealed tube. `S_(2)` : dry iodine reacts with ozone and formed yell

Description : `S_(1):(HPO_(3))_(n)` can be prepared by heating phosphorous acid and bromine in a sealed tube. `S_(2)` : dry iodine reacts with ozone and formed yell

Last Answer : `S_(1):(HPO_(3))_(n)` can be prepared by heating phosphorous acid and bromine in a sealed tube. `S_(2)` : ... below 369 K. A. FTF B. TTF C. TTT D. TFF

The number of S - S bonds in polythionic acid `(H_(2)S_(n)O_(6))`

Description : The number of S - S bonds in polythionic acid `(H_(2)S_(n)O_(6))`

Last Answer : The number of S - S bonds in polythionic acid `(H_(2)S_(n)O_(6))` A. n B. n - 1 C. n -2 D. None of these

In the reaction, `I_(2)+2S_(2)O_(3)^(2-) rarr 2I^(-)+S_(4)O_(6)^(2-)`. Equivalent wieght of iodine will be equal to

Description : In the reaction, `I_(2)+2S_(2)O_(3)^(2-) rarr 2I^(-)+S_(4)O_(6)^(2-)`. Equivalent wieght of iodine will be equal to

Last Answer : In the reaction, `I_(2)+2S_(2)O_(3)^(2-) rarr 2I^(-)+S_(4)O_(6)^(2-)`. Equivalent wieght of iodine ... B. Mol. wt./2 C. Mol. wt./4 D. None of these