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

1 Answer

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`

Related questions

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

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

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

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

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"`

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

Description : Tertiary butyl chloride preferably undergo hydrolysis by:

Last Answer : Tertiary butyl chloride preferably undergo hydrolysis by: A. `S_(N^(1))` mechanism B. `S_(N^(2))` mechanism C. and of (a) and (b) D. none of these

Description : Amides undergo hydrolysis under acidic conditions to give (a) Carboxylic acid and amine (b) Carboxylic acid and ammonium ion (c) Carboxylate ion and ammonium ion (d) Carboxylate ion and amine

Last Answer : Carboxylic acid and ammonium ion

Description : The compound that would undergo hydration very easily is

Last Answer : The compound that would undergo hydration very easily is A. `CH_(3)COCH_(2)Cl` B. `CH_(3)CH_(2)CHO` C. `Cl_3C-CHO` D. `Cl_(3)C CH_(2)COCH_(3)`

Description : A compound will be sensitive towards IR radiation only when one of the following properties undergo transition on (A) Polarizability (B) Dielectric constant (C) Dipole moment (D) Refractivity

Last Answer : (C) Dipole moment

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

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

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

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

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"):}`

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.

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.

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"):}`

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

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

Last 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)`

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

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

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`

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")`

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)

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`

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`

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

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

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`

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`

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)`

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]

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

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`

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

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

Description : `XeF_6` on partial hydrolysis with water produces a compound ‘X’. The same compound ‘X’ is formed when `XeF_6` reacts with silica. The compound ‘X’ Is

Last Answer : `XeF_6` on partial hydrolysis with water produces a compound X'. The same compound X' is formed when `XeF_6` ... XeF_4` C. (3)`XeF_2` D. (4)`XeOF_4`

Description : `Br_2+F_2` (excess)`to`A `overset("Hydrolysis")to` B+C The summation of atomicities of compound A, B and C is :

Last Answer : `Br_2+F_2` (excess)`to`A `overset("Hydrolysis")to` B+C The summation of atomicities of compound A, B and C is :

Description : Which of the following compound will not form during the hydrolysis of `XeF_(6)` ?

Last Answer : Which of the following compound will not form during the hydrolysis of `XeF_(6)` ? A. `XeO_(3)` B. `XeO_(4)` C. `XeOF_(4)` D. `XeO_(2)F_(2)`

Description : If an organic compound like glucose undergoes hydrolysis then the reaction is exergonic. True or false?

Last Answer : False. It cannot be exergonic considering the nature of the pyranose ring, a strong structure that requires high pressures and temperatures in order to break it. There is a reference from 1995 [Glucose ... ) is exergonic, that's the reason of why the body (in higher organisms) generates heat.

Description : If an organic compound like glucose undergoes hydrolysis then the reaction is exergonic. True or false?

Last Answer : False. It cannot be exergonic considering the nature of the pyranose ring, a strong structure that requires high pressures and temperatures in order to break it. There is a reference from 1995 [Glucose ... ) is exergonic, that's the reason of why the body (in higher organisms) generates heat.

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

Description : When ethyl acetoacetate is subjected to ketonic hydrolysis, the ketone obtained is (a) Dimethyl ketone (b) Methyl ethyl ketone (c) Diethyl ketone (d) Methyl n-propyl ketone

Last Answer : Diethyl ketone

Description : The ethyl derivative of acetoacetic ester on basic-hydrolysis gives (a) Acetic acid (b) Acetic acid and propionic acid (c) Propionic acid (d) Acetic acid and n-butyric acid

Last Answer : Acetic acid

Description : n-Propylmagnesium bromide on treatment with carbon dioxide and further hydrolysis gives : (a) Acetic acid (b) Propanoic acid (c) Butanoic acid (d) Formic acid

Last Answer : Butanoic acid

Description : Antibacterial agents can be classified with regard to their structure, mechanism of action, and activity pattern against various types of bacterial pathogens. Which of the following ... are both bacteriostatic d. Sulfonamides and trimethoprim act synergistically to inhibit purine synthesis

Last Answer : Answer: a, b, d Penicillins, cephalosporins, and monobactams possess a b-lactam ring of some type and act to bind bacterial division plate proteins, thus inhibiting cell wall ... act in different mechanisms to inhibit protein synthesis, therefore two agents in combination act synergistically

Description : Which compound reacts most rapidly by an SN1 mechanism? (a) Methyl chloride (b) Isopropyl chloride (c) Ethyl chloride (d) tert-Butyl chloride

Last Answer : tert-Butyl chloride

Description : The _________Protocol, addsa simple error control mechanism to the _______Protocol. A) Stop-and-Wait ARQ; Stop-and-Wait B) Go-Back-N ARQ; Stop-and-Wait C) Selective Repeat ARQ; Go-Back-N ARQ D) none of the above

Last Answer : Go-Back-N ARQ; Stop-and-Wait