Description : Arrange the following resonating structures in order of increasing stability `underset((I))(CH_(2)=overset(+)(N)=overset(-)(N))" "underset((II))(H_(2)
Last Answer : Arrange the following resonating structures in order of increasing stability `underset((I))(CH_(2)=overset(+)(N)= ... gt IV D. III gt I gt IV gt II
Description : The order of stability of the following carbocations: `underset("I")(CH_(2)C=CH-overset(o+)CH_(2))" , "underset("II")(CH_(3)-CH_(2)-overset(o+)CH_(2))
Last Answer : The order of stability of the following carbocations: `underset("I")(CH_(2)C=CH-overset(o+)CH_(2))" , "underset ... . II gt III gt I D. I gt II gt III
Description : The stability order in the following carbocations, `CH_(3)CH_(2)^(+)"(I), "(CH_(3))_(2)overset(+)CH"(II), "(CH_(3))_(3)C^(+)"(III) "overset(+)CH_(3)"(
Last Answer : The stability order in the following carbocations, `CH_(3)CH_(2)^(+)"(I), "(CH_(3))_( ... B. `IgtIIgtIIIgtIV` C. `IIIgtIVgtIgtII` D. `IIIgtIIgtIgtIV`
Description : Arrange the following in decreasing order of their stability :- `(I) CH_(3)-overset(oplus)(CH_(2)) " "(II) CH_(3)-underset(CH_(3))underset(|)overset(o
Last Answer : Arrange the following in decreasing order of their stability :- `(I) CH_(3)-overset(oplus)(CH_(2)) " "(II) CH_( ... II gt I` D. `III gt II gt I gt IV`
Description : Arrange the carbanions, `(CH_(3))_(3)bar(C),bar(C)Cl_(3),(CH_(3))_(2)bar(C)H,C_(6)H_(5)bar(C)H_(2)`, in order of their decreasing stability
Last Answer : Arrange the carbanions, `(CH_(3))_(3)bar(C),bar(C)Cl_(3),(CH_(3))_(2)bar(C)H,C_(6)H_(5)bar(C)H_(2 ... (2)bar(C)HgtC_(6)H_(5)bar(C)H_(2)gtbar(C)Cl_(3)`
Description : Arrange the following acid in decreasing order of their acidic strength : (I) `CH_(3)-OH` (II) `CH_(3)CH_(2)-OH` (III) `CH_(3)-underset(CH_(3))underse
Last Answer : Arrange the following acid in decreasing order of their acidic strength : (I) `CH_(3)-OH` (II) `CH_(3)CH_(2)- ... II gt IV` D. `II gt IV gt III gt I`
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 : What is the correct order of decreasing stability of the following cations ? `overset(oplus)underset(CH_(3)-CH-CH_(3)` II `overset(oplus)underset(CH_(
Last Answer : What is the correct order of decreasing stability of the following cations ? `overset(oplus)underset(CH_(3)-CH-CH_( ... gt I gt III D. II gt III gt I
Description : Arrange the following in correct order of their stability ? `(I) CH-=overset(Theta)C " "(II) CH_(2)=overset(Theta)CH " "(III) CH_(3)-overset(Theta)CH_
Last Answer : Arrange the following in correct order of their stability ? `(I) CH-=overset(Theta)C " "(II) CH_(2)=overset( ... gt III gt I` D. `II gt I gt III`
Description : Which of the following pairs of ions is more stable? (a) `CH_(3)CH_(2)O^(Ө)and CH_(2)=underset("(II)")(CH)-O^(Ө)` (b) `(CH_(3))_(2)underset("(I)")over
Last Answer : Which of the following pairs of ions is more stable? (a) `CH_(3)CH_(2)O^(Ө)and CH_(2)=underset("(II)" ... underset(..)O-CH=CH-CH=overset(o+)"N"Me_(2)`
Description : `(CH_(3))_(2)CHOH overset("Mild")underset("oxidation[O]")rarr (X) overset((i)CH_(3)Mgl)underset((ii)"Hydrolysis")rarr (Y)` In the above sequence of re
Last Answer : `(CH_(3))_(2)CHOH overset("Mild")underset("oxidation[O]")rarr (X) overset((i)CH_(3)Mgl) ... Iso butylene C. sec. Butyl alcohol D. tert. Butyl alcohol
Description : Arrange the following in increasing order as directed. `(a) (i) [CoCl_(3)(NH_(3))_(3)]," "(ii)[CoCl(NH_(3))_(5)]Cl_(2)," "(iii)[Co(NH_(3))_(6)]Cl_(3),
Last Answer : Arrange the following in increasing order as directed. `(a) (i) [CoCl_(3)(NH_(3))_(3)]," "(ii)[CoCl(NH_ ... -),NH^(3),NO^(3)^(-)`-strength of ligands.
Description : Arrange the following compounds in order of increasing molar conductivity . `(i) K[Co(NH_(3))_(2)(NO_(2))_(4)]" " (ii) [Cr(NH_(3))_(3)(NO_(2))_(3)]` `
Last Answer : Arrange the following compounds in order of increasing molar conductivity . `(i) K[Co(NH_(3))_(2)(NO_(2))_(4)]" ... )" " (iv) [Cr(NH_(3))_(6)]Cl_(3)`
Description : Which is the increasing order of acidic strength in the following compounds ? `CH_(3)CH_(2)CH_(2)COOH(I), "NCCH"_(2)COOH(II), H_(2)C=CHCH_(2)COOH(III)
Last Answer : Which is the increasing order of acidic strength in the following compounds ? `CH_(3)CH_(2)CH_(2) ... B. `IltIIIltII` C. `IIIltIIltI` D. `IIltIltIII`
Description : Among the following carbocations : (I) `Ph_(2)overset(+)"C"CH_(2)Me (II) PhCH_(2)CH_(2)overset(+)"C"HPh` `"(III) "Ph_(2)CHoverset(+)"C"HMe" (IV) "Ph_(
Last Answer : Among the following carbocations : (I) `Ph_(2)overset(+)"C"CH_(2)Me (II) PhCH_(2)CH_( ... B. `IgtIIgtIIIgtIV` C. `IIgtIgtIVgtIII` D. `IgtIVgtIIIgtII`
Description : Consider the following carbocations : (I) `C_(6)H_(5)overset(+)(C )H_(2)` (II) `C_(6)H_(5)CH_(2)overset(+)(C )H_(2)` (III) `C_(6)H_(5)overset(+)(C )HC
Last Answer : Consider the following carbocations : (I) `C_(6)H_(5)overset(+)(C )H_(2)` (II) `C_(6)H_(5)CH_(2)overset(+ ... lt I lt II lt IV D. IV lt III lt I lt II
Description : Arrange the following free radicals in increasing order of stability:
Last Answer : Arrange the following free radicals in increasing order of stability:
Description : The major product H in the given reaction sequence is `CH_(3)-CH_(2)-CO-CH_(3) overset(._(Theta)CN)toG overset(95% H_(2)SO_(4)) underset("Heat")toH`
Last Answer : The major product H in the given reaction sequence is `CH_(3)-CH_(2)-CO-CH_(3) overset(._(Theta)CN) ... CH=underset(CH_(3))underset(|)(C)-CO-NH_(2)`
Description : In the reaction , `(CH_(3))_(3)C CHO +HCHO overset(NaOH)underset("heat")toA+B` the products (A) and (B) are respectively
Last Answer : In the reaction , `(CH_(3))_(3)C CHO +HCHO overset(NaOH)underset("heat")toA+B` the products (A) and (B) ... (CH_(3))_(3)COONa` and `HCOO^(-) Na^(+)`
Description : `{:(" "O^(16)),(" ||"),(CH_(3)-C-H overset(D_(2)O^(18))underset(D^(o+))to CH_(3)-C-H),(" ||"),(" "._(18)O):}` Give the following reaction intermediate
Last Answer : `{:(" "O^(16)),(" ||"),(CH_(3)-C-H overset(D_(2)O^(18))underset(D^(o+))to CH_(3)-C-H),(" ||"),(" "._( ... ,(" |"),(CH_(3)-C-H),(" |"),(" "._(18)OD):}`
Description : `overset(1.Br_(2)(1"mole"), C CI_(4))underset(2.(CH_(3))_(2)NH("excess"))rarr A overset(1.CH_(3)I("excess"))underset(2.AgOH,Delta)rarr B` (Major produ
Last Answer : `overset(1.Br_(2)(1"mole"), C CI_(4))underset(2.(CH_(3))_(2)NH("excess"))rarr A overset(1.CH_(3) ... product) The major product (B) is: A. B. C. D.
Description : In the reaction `(CH_(3))_(3)C-O-CH_(2)CH_(3)+underset((1"mole"))(HI)overset(heat)(rarr)` the products formed is (are)
Last Answer : In the reaction `(CH_(3))_(3)C-O-CH_(2)CH_(3)+underset((1"mole"))(HI)overset(heat)(rarr)` the products ... (H)underset(|)O^(+)-CH_(2)CH_(3)I^(-)`
Description : Arrangements of `(CH_(3))_(3)C-,(CH_(3))_(2)CH-,CH_(3).CH_(2)-` when attached to benzyl or `n` unsaturated group in increasing order of inductive effe
Last Answer : Arrangements of `(CH_(3))_(3)C-,(CH_(3))_(2)CH-,CH_(3).CH_(2)-` when attached to benzyl or `n` unsaturated ... C- lt CH_(3)CH_(2)- lt(CH_(3))_(2)CH-`
Description : Arrange the following compounds in decreasing order of reactivity for EAR :- (I) `CH_(2)=CH_(2)` (II) `CH_(3)-CH=CH_(2)` (III) `Ph_(2)C=CH-CH_(3)` (IV
Last Answer : Arrange the following compounds in decreasing order of reactivity for EAR :- (I) `CH_(2)=CH_(2)` (II) `CH_(3)- ... I gt IV` D. `II gt III gt IV gt I`
Description : Arrange the compounds in order of decreasing acidic strength : (I) `ClCH_(2)-CH_(2)-OH` (II) `Cl_(2)CH-CH_(2)-OH` (III) `Cl-CH_(2)-CH_(2)-CH_(2)-OH` (
Last Answer : Arrange the compounds in order of decreasing acidic strength : (I) `ClCH_(2)-CH_(2)-OH` (II) `Cl_(2)CH-CH_(2 ... IV gt III` D. `II gt I gt III gt IV`
Description : Arrange the following free radicals in order of decreasing stability: Methyl(I), Vinly(II), Allyl(III), Benzyl(IV)
Last Answer : Arrange the following free radicals in order of decreasing stability: Methyl(I), Vinly(II), Allyl(III), Benzyl(IV) ... gt III D. IV gt III gt I gt II
Description : The order of acidic strength of the hydrogen atom `(H_(alpha), H_(beta), H_(gamma))` in the given molecule is : `CH_(3)-underset(H_(beta))underset(|)(
Last Answer : The order of acidic strength of the hydrogen atom `(H_(alpha), H_(beta), H_(gamma))` in the given molecule ... D. `H_(beta)gt H_(alpha) gt H_(gamma)`
Description : `Ph-CH=CH-underset(O)underset(C)-H overset((i) CH_(3)CH_(2)MgBr)to overset((ii) H_(3)O^(o+))to(X) overset(Cu,Delta)to(Y)`
Last Answer : `Ph-CH=CH-underset(O)underset(C)-H overset((i) CH_(3)CH_(2)MgBr)to overset((ii) H_(3)O^(o+))to(X) ... -underset(O)underset(||)(C)-CH=CH-CH_(2)-CH_(3)`
Description : In the given reaction `{:(" "CH_(3)),(" |"),(H_(3)C-C-C-CHO),(" | ||"),(" "H_(3)C " "O):} overset("(i)Conc. NaOH")underset((ii)H^(+)) to` product is
Last Answer : In the given reaction `{:(" "CH_(3)),(" |"),(H_(3)C-C-C-CHO),(" | ||"),(" "H_(3)C " "O):} overset("(i) ... )C-C-C-CH_2),(" | ||"),(" "H_(3)C " "OH):}`
Description : `CH_(3)COOH overset((i) PCl_(3)+Cl_(2) ("excess"))underset((ii) O_(2))to (X) overset(SOCl_2) to (Y) overset(H_(2)//Pd//BaSO_(4))to(Z) overset(OH^(-))t
Last Answer : `CH_(3)COOH overset((i) PCl_(3)+Cl_(2) ("excess"))underset((ii) O_(2))to (X) overset(SOCl_2) to (Y) ... W+S ` Write the structure of X,Y,Z , W and S
Description : For the given compound `CH_(3)-underset(overset(|)(OH))(CH)-CH=CH-CH_(3).` (i) Total number of stereoisomers. (ii) Number of opticallly active stereoi
Last Answer : For the given compound `CH_(3)-underset(overset(|)(OH))(CH)-CH=CH-CH_(3).` ... number of fractions on fractional distillation of all stereoisomers.
Description : Consider the following structure `{:(underset("I")(CH_(2)C=overset(+)CH)" , "underset("II")(CH_(3)-overset(+)CH_(2))),(underset("III")(H_(2)C=CH-overs
Last Answer : Consider the following structure `{:(underset("I")(CH_(2)C=overset(+)CH)" , "underset("II")(CH_(3)-overset(+) ... C. `IV,II,III,I` D. `I,III,II,IV`
Description : In the given reaction `CH_(3)-CH_(2)-NH-CH_(2)-CH_(2)-CI overset((i)CH_(3)I ("excess"))underset((ii)AgOH//Delta)rarr[X]` is the major product, [X] wil
Last Answer : In the given reaction `CH_(3)-CH_(2)-NH-CH_(2)-CH_(2)-CI overset((i)CH_(3)I ("excess"))underset((ii)AgOH// ... of (a) and (b) D. `CH_(3) -CH_(2)-CI`
Description : Reactivity order of the following alkenes for hydrochlorination (HCl) is (I) `CH_(2) = CH - Cl` (II) `(CH_(3))_(2)C=CH_(2)` (III) `CH_(2) = CH - CHO`
Last Answer : Reactivity order of the following alkenes for hydrochlorination (HCl) is (I) `CH_(2) = CH - Cl` (II) `(CH_(3) ... `II gt I gt III` D. `III gt I gt II`
Description : Correct order of basic strength in gas phase is (I) `CH_(3)-NH_(2)` (II) `(CH_(3))_(2)NH` (III) `(CH_(3))_(3)N` (IV) `NH_(3)`
Last Answer : Correct order of basic strength in gas phase is (I) `CH_(3)-NH_(2)` (II) `(CH_(3))_(2)NH` (III) `(CH_(3))_(3 ... C` C. `A gt C gt B` D. `C gt A gt B`
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 : Arrange the following religious groups in increasing order of their population in India: 1. Muslims 2. Buddhists 3. Sikhs 4. Jains 5. Christians (a) IV, II, III, V, I (b) IV, II, I, III, V (c) II, IV, III, V, I (d) II, III, IV, I,V
Last Answer : Ans: (a)
Description : Arrange the following in correct order of reactivity towards `Cl_(2)//hupsilon` (A) `CH_(4)` (B) `CH_(3)CH_(3)` (C ) `CH_(3)CH_(2)CH_(3)` (D) `CH_(3)-
Last Answer : Arrange the following in correct order of reactivity towards `Cl_(2)//hupsilon` (A) `CH_(4)` (B) `CH_(3)CH_(3)` ( ... gt A gt D` D. `C gt B gt D gt A`
Description : Arrange `CFC, CH_(4), N_(2)O, and CO_(2)` in decreasing order according to their contribution in greenhouse effect:
Last Answer : Arrange `CFC, CH_(4), N_(2)O, and CO_(2)` in decreasing order according to their contribution in greenhouse ... (2)` D. `CO_(2)gtCH_(4)gtCFCgtN_(2)O`
Description : Arrange the following carbanions in decreasing orde of stability: `HC-=bar(C)(I)," "H_(3)C-C-=bar(C)(II),` `H_(2)C=bar(C)H(III)," "H_(3)C-bar(C)H_(2)(
Last Answer : Arrange the following carbanions in decreasing orde of stability: `HC-=bar(C)(I)," "H_(3 ... `IIgtIgtIIIgtIV` C. `IVgtIIIgtIIgtI` D. `IgtIIgtIIIgtIV`
Description : `CH_(2)=CH-CH_(2)-CH_(2)-C-=CH underset((1 eq))overset(HBr)to ` Product is
Last Answer : `CH_(2)=CH-CH_(2)-CH_(2)-C-=CH underset((1 eq))overset(HBr)to ` Product is A. `BrCH_(2)-CH_(2)- ... (3)-underset(Br)underset(|)CH-CH_(2)-CH_(2)-C-=CH`
Description : `CH_(3) equiv C CH_(3) overset(Na, NH_(3) (i))(rarr) Q overset("dil. Cold")underset(KMnO_(4))(rarr) R` If Q is an unsaturated hydrocarbon then product
Last Answer : `CH_(3) equiv C CH_(3) overset(Na, NH_(3) (i))(rarr) Q overset("dil. Cold")underset(KMnO_(4))(rarr) R` If ... ii & iii B. i & ii C. only v D. only iv
Description : In following compound `CH_(3)-CH_(2)-underset(CH_(3))overset(CH_(3))underset|overset(|)(C)-underset(CH_(3))underset(|)(CH)-overset(CH_(3))overset(|)(C
Last Answer : In following compound `CH_(3)-CH_(2)-underset(CH_(3))overset(CH_(3))underset|overset(|)(C)-underset(CH_(3))underset(|)( ... ,5,5 C. 4,5,3,3 D. 5,5,4,3