Description : Arragne basicity of the following compounds in decreasing order: `CH_(3)CH_(2)NH_(2)(I)," "H_(2)C=CH-NH_(2)(II),` `HC-=C-NH_(2)(III)," "C_(6)H_(5)NH_(
Last Answer : Arragne basicity of the following compounds in decreasing order: `CH_(3)CH_(2)NH_(2)(I), ... `IVgtIIIgtIIgtI` C. `IIIgtIIgtIgtIV` D. `IgtIIIgtIIgtIV`
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 : 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 : An organic compound A,`C_(5)H_(8)O` reacts with `H_(2)O, NH_(3)` and `CH_(3)COOH` as described below A is
Last Answer : An organic compound A,`C_(5)H_(8)O` reacts with `H_(2)O, NH_(3)` and `CH_(3)COOH` as described ... 2))underset(||)(C)-underset(H)underset(|)(C)=O`
Description : The reaction `RCH_(2)CH_(2)COOH overset(Red P)underset(Br_(2))toRCH_(2)-underset(Br)underset(|)(C)HCOOH` is called as
Last Answer : The reaction `RCH_(2)CH_(2)COOH overset(Red P)underset(Br_(2))toRCH_(2)-underset(Br) ... reaction C. Reimer Teimann reaction D. Sandmeyer reaction
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 : Which is the decreasing oreder of acidity in the following compounds? `{:(CH_(3)CH_(2)OH"(I) "CF_(3)CH_(2)OH"(II)"),("CCl"_(3)-CH_(2)OH"(III) "(NO_(2)
Last Answer : Which is the decreasing oreder of acidity in the following compounds? `{:(CH_(3)CH_(2)OH ... `IIgtIgtIIIgtIV` C. `IVgtIIgtIgtIII` D. `IVgtIIgtIIIgtI`
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 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 : `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 : The product P of the following reaction is `CH_(3)-COOH overset(LiAlH_(4))to overset(SOCl_(2))to overset(Koverset(14)(C)N)to overset(H_(3)O^(o+)) to P
Last Answer : The product P of the following reaction is `CH_(3)-COOH overset(LiAlH_(4))to overset(SOCl_(2))to overset(Koverset ... )N)to overset(H_(3)O^(o+)) to P`
Description : Condiser the reactions, (i) `(CH_(3))_(2)CH-CH_(2)Broverset(C_(2)H_(5)OH)rarr(CH_(3))_(2)CH-CH_(2)OC_(2)H_(5)+HBr` (ii) `(CH_(3))_(2)CH-CH_(2)Broverse
Last Answer : Condiser the reactions, (i) `(CH_(3))_(2)CH-CH_(2)Broverset(C_(2)H_(5)OH)rarr(CH_(3))_(2)CH-CH_(2)OC_(2)H_(5) ... N^(1))` D. `S_(N^(2)) and S_(N^(2))`
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 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 : The correct order of decreasing basicity of the following species is: `H_(2)O, OH^(-), CH_(3)OH, CH_(3)O`
Last Answer : The correct order of decreasing basicity of the following species is: `H_(2)O, OH^(-), CH_(3)OH, CH_(3)O` A. ... CH_(3)O^(-) gt CH_(3)OH gt H_(2)O`
Description : What is the product when `C_(6)H_(5)CH_(2)NH_(2)` reacts with `HNO_(3)`?
Last Answer : What is the product when `C_(6)H_(5)CH_(2)NH_(2)` reacts with `HNO_(3)`?
Description : In the given reaction which one of the following statement is correct - `C_(6)H_(5)-underset(CH_(3))underset(|)(C)=O+NH_(2)-OH to "Oxime" overset(PCl_
Last Answer : In the given reaction which one of the following statement is correct - `C_(6)H_(5)- ... elimination reaction. D. oxime and amides are isomers.
Description : `C_(6)H_(5)-CH_(2)-I overset(NaN_(3))underset(Delta)rarr` Products Reaction is assumed to involve nitrene as intermediate, then various possible produ
Last Answer : `C_(6)H_(5)-CH_(2)-I overset(NaN_(3))underset(Delta)rarr` Products Reaction is assumed to involve nitrene as ... (2)` C. `C_(6)H_(5)CN=NH` D.
Description : In the given reaction sequence `C_(6)H_(5)-CH_(2)-NH_(2) overset(CHCl_(3)//Alc.KOH)underset(Delta)rarr [X] overset(H_(2)O //NaOH)rarr [Y],[Y]` will be
Last Answer : In the given reaction sequence `C_(6)H_(5)-CH_(2)-NH_(2) overset(CHCl_(3)//Alc.KOH)underset(Delta)rarr [X] ... -NH_(2)` D. `C_(6)H_(5)-CH_(2)OH`
Description : How many of the following compounds would give Iodoform test (1) `s CH_(3) - CO - CH_(2) - CO - OCH_(3)` (2) `C_(6) H_(5) - CO - CH_(2) - CO - C_(6)H_
Last Answer : How many of the following compounds would give Iodoform test (1) `s CH_(3) - CO - CH_(2) - CO - OCH_(3)` (2 ... `CH_(3) - CO - CH_(2) - CHOH - CH_(3)`
Description : `C_(6)H_(5)Ohoverset(CH_(3)COCl)underset(NaOH(aq))(rarr)C_(6)H_(5)OCOCH_(3)` the above reaction is an example of
Last Answer : `C_(6)H_(5)Ohoverset(CH_(3)COCl)underset(NaOH(aq))(rarr)C_(6)H_(5)OCOCH_(3)` ... reaction B. Schotten-Baumann reaction C. Acetylation D. Benzoylation
Description : `C_(6)H_(5)-O-CH_(2)CH_(3)overset(HI)rarr` which of the following is not formed in this reaction ?
Last Answer : `C_(6)H_(5)-O-CH_(2)CH_(3)overset(HI)rarr` which of the following is not formed in this reaction ? A. ... )H_(5)-OH` C. Both of these D. None of these
Description : `C_(6)H_(5)-O-CH_(3)+HI_((excess))rarr`
Last Answer : `C_(6)H_(5)-O-CH_(3)+HI_((excess))rarr` A. `CH_(3)OH and C_(6)H_(5)I` B. `CH_(3)I and C_(6)H_(5)OH` ... )I and C_(6)H_(5)I` D. `C_(6)H_(6) and CH_(4)`
Description : Which of the following structures correspond to the product expected, when excess of `C_(6)H_(6)` reacts with `CH_(2)Cl_(2)` in presence of anhydrous
Last Answer : Which of the following structures correspond to the product expected, when excess of `C_(6)H_(6)` reacts with ` ... anhydrous `AlCl_(3)`? A. B. C. D.
Description : In the following compounds phenol (I), p-cresol (II), m-nitrophenol (III) and p-nitrophenol (IV), the order of acidity is:
Last Answer : In the following compounds phenol (I), p-cresol (II), m-nitrophenol (III) and p- ... `IgtIVgtIIIgtII` C. `IIgtIgtIIIgtIV` D. `IVgtIIIgtIgtII`
Description : Given that standard heat enthalpy of `CH_(4), C_(2)H_(4)` and `C_(3)H_(8)` are -17.9, 12.5, -24.8 Kcal/mol. The `Delta H` for `CH_(4)+C_(2)Hrarr C_(3)
Last Answer : Given that standard heat enthalpy of `CH_(4), C_(2)H_(4)` and `C_(3)H_(8)` are -17.9, 12.5, -24.8 Kcal ... . `-30.2` Kcal C. 55.2 Kcal D. `-19.4` Kcal
Description : Consider the given compounds : (a) `CH_(3)-CH_(2)-NH_(2)` (b) `CH_(3)-CH=NH` (c ) `CH_(3)-C=N` (d) `C_(2)H_(5)-NH-C_(2)H_(5)` Arrange basicity of thes
Last Answer : Consider the given compounds : (a) `CH_(3)-CH_(2)-NH_(2)` (b) `CH_(3)-CH=NH` (c ) `CH_(3)-C=N` (d) `C_(2 ... `a gt d gt b gt c` D. `d gt a gt c gt b`
Description : Write down the IUPAC names of the following compounds :- (A) `CH_(3)-underset(C_(2)H_(5))underset(|)(CH)-overset(CH_(3))overset(|)(CH)-underset(OH)und
Last Answer : Write down the IUPAC names of the following compounds :- (A) `CH_(3)-underset(C_(2)H_(5))underset(|)( ... )=CH-underset(CH_(3))underset(|)(CH)-C-=CH`
Description : The reaction of compounf P with `CH_(3)MgBr` (excess) in `(C_(2)H_(5)_(2)O` followed by addition of `H_(2)O` give Q the compound Q on treatment with `
Last Answer : The reaction of compounf P with `CH_(3)MgBr` (excess) in `(C_(2)H_(5)_(2) ... and Friedel-Crafts acylation D. Dehydration and Friedel-Crafts acylation
Last Answer : The reaction of compounf P with `CH_(3)MgBr` (excess) in `(C_(2)H_(5)_(2)O` followed by addition of `H_ ... product S is The product S is A. B. C. D.
Description : The end product (B) of the reaction sequence: `C_(2)H_(5)-underset(H)underset(|)(N)-CH_(3) overset(Ph-overset(O)overset(||)(C)-Cl)underset(NaOH)rarrA
Last Answer : The end product (B) of the reaction sequence: `C_(2)H_(5)-underset(H)underset(|)(N)-CH_(3) overset(Ph-overset ... )underset(H_(2)O)rarr B` A. B. C. D.
Description : Assertion: (A) Ethers are relatively inert when compared to `C_(2)H_(5)OH` Reason (R): The hybridization of C and O in `CH_(3)-O-CH_(3) is SP^(3)`
Last Answer : Assertion: (A) Ethers are relatively inert when compared to `C_(2)H_(5)OH` Reason (R): The hybridization of ... R is false D. A is false but R is true
Description : Which alkyl halide would be preferred for the synthesis of the following ether by Williamson synthesis ? `H_(5)C_(2)-O-overset(CH_(3))overset(|)unders
Last Answer : Which alkyl halide would be preferred for the synthesis of the following ether by Williamson ... chloride C. Ethyl chloride D. Methyl chloride
Description : The IUPAC name of `C_(2)H_(5)-O-CH(CH_(3))_(2)`
Last Answer : The IUPAC name of `C_(2)H_(5)-O-CH(CH_(3))_(2)` A. Ethoxy propane B. 1,1-dimenthyl ether C. 2- Ethoxy isopropane D. 2-Ethoxy propane
Description : `C_(2)H_(5)OH overset(KMnO_(4)//H^(oplus))rarrX underset(H_(2)SO_(4))overset(Y)rarr CH_(3)COOC_(2)H_(5)`, X and Y respectively are
Last Answer : `C_(2)H_(5)OH overset(KMnO_(4)//H^(oplus))rarrX underset(H_(2)SO_(4))overset(Y)rarr CH_(3)COOC_(2)H_(5)` ... CH_(3)COOH` D. `CH_(3)COOH, C_(2)H_(5)OH`
Description : The decreasing order of acidity among the following compounds is : `underset("(I)")("ethanol"), underset("(II)")("2,2,2-trifluoroethanol"),underset("(
Last Answer : The decreasing order of acidity among the following compounds is : `underset("(I)")("ethanol"), underset("(II)")( ... IV gt I D. I gt II gt III gt IV
Description : The heat of combustion of `CH_(4(g)), C_((g))` and `H_(2(g))` at `25^(@)C` are `-212.4` K cal, -94.0 K cal and -68.4 K cal respectively, the heat of f
Last Answer : The heat of combustion of `CH_(4(g)), C_((g))` and `H_(2(g))` at `25^(@)C` are `-212.4` K cal, -94.0 ... .4` K cal C. `-375.2` K cal D. `+212.8` K cal
Description : Among the complex ions, `[Co(NH_(2) - CH_(2) - CH_(2) - NH_(2))_(2) Cl_(2)]^(+), [CrCl_(2) (C_(2)O_(4))_(2)]^(3-)` `[Fe(H_(2)O)_(4) (OH)_(2)]^(+), [Fe
Last Answer : Among the complex ions, `[Co(NH_(2) - CH_(2) - CH_(2) - NH_(2))_(2) Cl_(2)]^(+), [CrCl_(2) ... (3)) Cl]^(2+)` and that show(s) cis-trans isomerism is
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 : 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 : Find the the valency factor for following acids `(i) CH_(3)CO OH " " (ii) NaH_(2)PO_(4) " " (iii) H_(3)BO_(3)`
Last Answer : Find the the valency factor for following acids `(i) CH_(3)CO OH " " (ii) NaH_(2)PO_(4) " " (iii) H_(3)BO_(3)`
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 : 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 : 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 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 : 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 : Among the following anions, the order of basicity is : `overset(-)(C )H_(3)(I), overset(-)(N)H_(2)(II), OH^(-)(III),F^(-)(IV)`
Last Answer : Among the following anions, the order of basicity is : `overset(-)(C )H_(3)(I), overset(-)(N)H_(2)(II), OH^(- ... > II > I > IV D. III > I > II > IV