The acid D obtained through the following sequence of reactions is: `C_(2)H_(5)Br overset(Alc. KOH)rarrA overset(Br_(2))underset(C Cl_(4))rarrBoverset

1 Answer

Answer :

The acid D obtained through the following sequence of reactions is: `C_(2)H_(5)Br overset(Alc. KOH) ... B. Malonic acid C. Maleic acid D. Oxalic acid

Related questions

Description : The acid D obtained through the following sequence of reactions is: `C_(2)H_(5)Br overset(Alc. KOH)rarrA overset(Br_(2))underset(C Cl_(4))rarrBoverset

Last Answer : The acid D obtained through the following sequence of reactions is: `C_(2)H_(5)Br overset(Alc. KOH) ... B. Malonic acid C. Maleic acid D. Oxalic acid

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 : Consider the following sequence of reactions : `H_(2)C = CH-CH =CH_(2) overset(Br_(1)(1 "mole"))underset(C CI_(4))rarrA overset(1.KCN("excess"))unders

Last Answer : Consider the following sequence of reactions : `H_(2)C = CH-CH =CH_(2) overset(Br_(1)(1 "mole"))underset(C ... ))underset(|)(CH)-(CH_(2))_(2)-NH_(2)`

Description : The product B of the following sequence of reactions is `C_(6)H_(5)CONH_(2) overset(Br_(2))underset(NaOH)toA overst(NaNO_(2)//HCl)underset(ul(" "0-5^(

Last Answer : The product B of the following sequence of reactions is `C_(6)H_(5)CONH_(2) overset(Br_(2))underset(NaOH)toA overst( ... 5^(@)C" "))toB` 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 : `CH_(3)-CH_(2)-CH_(2)-underset(OH)underset(|)(CH)-CH_(3) underset(-H_(2)O)overset(H^(o+))rarr[F] overset(Br_(2)//C Cl_(4))rarrC_(5)H_(10)Br_(2)(G)` Ho

Last Answer : `CH_(3)-CH_(2)-CH_(2)-underset(OH)underset(|)(CH)-CH_(3) underset(-H_(2)O)overset(H^(o+))rarr[F] ... (including all stereoisomers) A. 2 B. 6 C. 3 D. 5

Description : `overset(1.Br_(2)^(-)+KOH, Delta)underset(2.H_(3)O^(o+))rarr` The product of above reaction is:

Last Answer : `overset(1.Br_(2)^(-)+KOH, Delta)underset(2.H_(3)O^(o+))rarr` The product of above reaction is: A. B. C. D.

Description : Consider the following sequence of reactions: `overset(C CI_(4))underset(Delta)rarr A overset(1.CH_(2)=CH-CH_(2)Br)underset(2.H_(3)O^(o+),Delta)rarrB`

Last Answer : Consider the following sequence of reactions: `overset(C CI_(4))underset(Delta)rarr A overset(1.CH_(2)=CH-CH_(2) ... end product (B) is: A. B. C. D.

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 : `CH_(3)CH_(2)-CH_(2)-COOH overset("Red + P" +Br_(2))toCH_(3)-CH_(2)-underset(Br)underset(|)(CH)-COOH` This reaction is called

Last Answer : `CH_(3)CH_(2)-CH_(2)-COOH overset("Red + P" +Br_(2))toCH_(3)-CH_(2)-underset(Br)underset(|)(CH)-COOH` This reaction is called

Description : `CH_(3)CH_(2)-CH_(2)-COOH overset("Red + P" +Br_(2))toCH_(3)-CH_(2)-underset(Br)underset(|)(CH)-COOH` This reaction is called

Last Answer : `CH_(3)CH_(2)-CH_(2)-COOH overset("Red + P" +Br_(2))toCH_(3)-CH_(2)-underset(Br)underset(|)(CH)-COOH` This reaction is called

Description : End product of the following reaction is `CH_(3)CH_(2)COOH overset(Cl_(2))underset(red P)to overset("alcoholic KOH")to`

Last Answer : End product of the following reaction is `CH_(3)CH_(2)COOH overset(Cl_(2))underset(red P)to overset(" ... |)(C)H_(2)underset(OH)underset(|)(C)HCOOH`

Description : The correct statement(s) about the following reaction sequence is (are) Cumene `(C_(9)H_(12))underset((ii)H_(3)O^(+))overset((i)O_(2))rarrPoverset(CHC

Last Answer : The correct statement(s) about the following reaction sequence is (are) Cumene `(C_(9)H_(12) ... violet coloration with 1% aqueous `FeCl_(3)` solution

Description : The major product (B) formed in the reaction sequence is: `overset(Ph-overset(O)overset(||)(C)-CI)underset(dil.NaOH)rarrA overset(1.CH_(3)MgBr)underse

Last Answer : The major product (B) formed in the reaction sequence is: `overset(Ph-overset(O)overset(||)(C)-CI)underset(dil. ... )overset(||)(C)-CH_(3)` B. C. D.

Description : Compound (A), `C_(10)H_(12)O` gives off hydrogen on treatment with sodium metal and decolourises `Br_(2)` in `C Cl_(4)` to give (B), `C_(10)H_(12)OBr`

Last Answer : Compound (A), `C_(10)H_(12)O` gives off hydrogen on treatment with sodium metal and ... pairs of diasteereomers D. A has 2 chiral centres

Description : A `C_(6)H_(12)O` compound does not react with `Br_(2)` in `C Cl_(4)`, produces a flammable gas on treatment with `LiAlH_(4)`, and reacts with `H_(2)Cr

Last Answer : A `C_(6)H_(12)O` compound does not react with `Br_(2)` in `C Cl_(4)`, ... B. methoxycyclopentane C. 2-cyclopropyl-2-propanol D. 2-cyclobutylethanol

Description : Identify the product Z in the following sequence of reactions "`phenol" overset(NaOH)rarrX underset(4-7 atm, 410 K)overset(CO_(2))rarrY overset(H_(3)O

Last Answer : Identify the product Z in the following sequence of reactions "`phenol" overset(NaOH)rarrX ... Salicyladehyde C. Benzoic acid D. Salicylic acid

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 : `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 : Reaction I `Ph-overset(O)overset(||)(C)-NH_(2) overset(overset(Theta)(OD),Br_(2))rarrA` Reaction II `Ph-overset(O)overset(||)(C)-ND_(2) overset(overse

Last Answer : Reaction I `Ph-overset(O)overset(||)(C)-NH_(2) overset(overset(Theta)(OD),Br_(2))rarrA` Reaction II `Ph- ... Both `Ph-NH_(2)` D. Both `Ph-ND_(2)`

Description : `CH_(3)CH_(2)Br overset(AgCN)rarr A overset(NaOH, Delta)underset(overset(o+)(H_(3)O))rarrB,(B)` is:

Last Answer : `CH_(3)CH_(2)Br overset(AgCN)rarr A overset(NaOH, Delta)underset(overset(o+)(H_(3)O))rarrB,(B)` is: A. `CH_( ... (2)NH_(2)` C. `CH_(3)CH_(2)NH_(2)` D.

Description : Write the product of following reactions `(a) CH_3-CH_(2)-OH overset(I_(2)//KOH)to "" Ph-CH_(2)-CO-CH_(3)overset(I_(2)//KOH)to` (c) CH_(3)-underset(OH

Last Answer : Write the product of following reactions `(a) CH_3-CH_(2)-OH overset(I_(2)//KOH)to "" Ph-CH_(2)-CO- ... (OH)underset(|)(CH)-Ph overset(I_(2)//KOH)to`

Description : Write the product of following reactions `(a) CH_3-CH_(2)-OH overset(I_(2)//KOH)to "" Ph-CH_(2)-CO-CH_(3)overset(I_(2)//KOH)to` (c) CH_(3)-underset(OH

Last Answer : Write the product of following reactions `(a) CH_3-CH_(2)-OH overset(I_(2)//KOH)to "" Ph-CH_(2)-CO- ... (OH)underset(|)(CH)-Ph overset(I_(2)//KOH)to`

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 : `C_(6)H_(5)NH_(2) overset(NaNO_(2)+HCl)underset(0-5^(@)C) X overset(H_(2)O)underset(Delta)toY,` the product is :

Last Answer : `C_(6)H_(5)NH_(2) overset(NaNO_(2)+HCl)underset(0-5^(@)C) X overset(H_(2)O) ... : A. Benzenediazonium chloride B. Nitrobenzene C. Phenol D. Cresol

Description : In the reaction, `C_(6)H_(5)NH_(2)underset(0-5^(@)C)overset(NaNO_(2)+HCl)rarr(A)underset(KCN)overset(CuCN)rarr(B)overset(H^(+)//H_(2)O)rarr(C)` the pr

Last Answer : In the reaction, `C_(6)H_(5)NH_(2)underset(0-5^(@)C)overset(NaNO_(2)+HCl)rarr(A)underset(KCN)overset(CuCN ... COOH` C. `C_(6)H_(5)OH` D. none of these

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 : 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 : `C_(2)H_(5)-O-C_(2)H_(5)+underset(excees)HI overset(Delta)underset((hot))rarrX+Y` here X and Y are

Last Answer : `C_(2)H_(5)-O-C_(2)H_(5)+underset(excees)HI overset(Delta)underset((hot))rarrX+Y` here X and Y are A. `C_(2)H_ ... 5)OH+H_(2)O` D. `C_(2)H_(4)+H_(2)O`

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 major product formed in the reaction: `overset(p-TsOH("Trace"))underset(C_(6)H_(6).Delta)rarr`

Last Answer : The major product formed in the reaction: `overset(p-TsOH("Trace"))underset(C_(6)H_(6).Delta)rarr` A. B. C. D.

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 : `"phenol" overset(conc.H_(2)SO_(4))rarrA overset(conc.HNO_(3))rarrB` Here A and B are respectively.

Last Answer : `"phenol" overset(conc.H_(2)SO_(4))rarrA overset(conc.HNO_(3))rarrB` Here A and B ... 4-dinitrophenol D. 3-Hydroxybenzene sulphonic acid, picric acid

Description : How many of these reactions are homogeneously catalyzed ? (i) `2SO_(2)(g) + O_(2)(g) overset(NO(g))to 2SO_(3)(g)` (ii) `C_(12)H_(22)O_(11)(aq.) + H_(2

Last Answer : How many of these reactions are homogeneously catalyzed ? (i) `2SO_(2)(g) + O_(2)(g) overset(NO(g))to ... (2)(g)overset(Ni(s))to` Vegetable ghee (s).

Description : In the sequence of reaction (A) is `(A)overset(Na)rarr` (B) `overset(C_(2)H_(5)I//heat)rarr` (C) `overset(HI//heat)rarr C_(2)H_(5)I`

Last Answer : In the sequence of reaction (A) is `(A)overset(Na)rarr` (B) `overset(C_(2)H_(5)I//heat) ... acid B. Methyl alcohol C. Ethyl alcohol D. Propionic acid

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 : P and Q are isomer of dicraboxylic acid `C_(4)H_(4)O_(4)` Both decolourixe `Br_(2)//H_(2)O`. On heating , P forms the cyclic anhydride. Upon treatment

Last Answer : P and Q are isomer of dicraboxylic acid `C_(4)H_(4)O_(4)` Both decolourixe `Br_(2)//H_(2)O`. On ... sequences V and W are respectively A. B. C. D.

Description : `P` and `Q` are isomers of dicarboxylic acid `C_(4)H_(4)O_(4)`. Bothdecolorize `Br_(2)//H_(2)O`. On heating, `P` forms the cyclic anhydride. Upon trea

Last Answer : `P` and `Q` are isomers of dicarboxylic acid `C_(4)H_(4)O_(4)`. Bothdecolorize `Br_(2)// ... . Optically inactive pair (T, U) and optically inactive S

Description : How many sterioisomers does the following compound have ? `CH_(3)-CH_(2)-underset(overset(|)(Br))(C)H-CH_(2)-CH=CH-CH_(3)`

Last Answer : How many sterioisomers does the following compound have ? `CH_(3)-CH_(2)-underset(overset(|)(Br))(C)H-CH_(2)-CH=CH-CH_(3)` A. None B. 2 C. 4 D. 6

Description : How many sterioisomers does the following compound have ? `CH_(3)-CH_(2)-underset(overset(|)(Br))(C)H-CH_(2)-CH=CH-CH_(3)`

Last Answer : How many sterioisomers does the following compound have ? `CH_(3)-CH_(2)-underset(overset(|)(Br))(C)H-CH_(2)-CH=CH-CH_(3)` A. None B. 2 C. 4 D. 6

Description : Total number of stereoisomers of compound is: `CH_(3)-underset(overset(|)(OH))(C)H-underset(overset(|)(Br))(C)H-CH_(3)`

Last Answer : Total number of stereoisomers of compound is: `CH_(3)-underset(overset(|)(OH))(C)H-underset(overset(|)(Br))(C)H-CH_(3)` A. 2 B. 4 C. 6 D. 8

Description : Number of chiral carbon persent in the following compound: `CH_(3)-underset(overset(|)(OH))(C)H-CH_(2)-underset(overset(|)(Br))(C)H-underset(overset(|

Last Answer : Number of chiral carbon persent in the following compound: `CH_(3)-underset(overset(|)(OH))(C)H-CH_(2)-underset(overset( ... (3)` A. 2 B. 3 C. 4 D. 5

Description : Compound (A) `C_(8)H_(9)Br`, gives a white precipitate when warmed with alcoholic `AgNO_(3)`. Oxidation of (A) gives an acid (B),`C_(8)H_(6)O_(4)`. (B

Last Answer : Compound (A) `C_(8)H_(9)Br`, gives a white precipitate when warmed with alcoholic `AgNO_(3)`. Oxidation of ... . Identify the compound (A) A. B. C. D.

Description : Predict the nature of the product `PC_(6)H_(5)CONH_(2) overset(Br_(2)//PD^(-))rarr P`

Last Answer : Predict the nature of the product `PC_(6)H_(5)CONH_(2) overset(Br_(2)//PD^(-))rarr P` A. `C_(6)H_(5)NH_ ... NHD` C. `C_(6)H_(5)ND_(2)` D. All of these

Description : `Ph-overset(O)overset(||)(C)-NH_(2)+Ph-CH_(2)-overset(O)overset(||)(C)-overset(15)(N)H_(2) overset(overset(Theta)(OH)+Br_(2))rarr A+B` Products A and

Last Answer : `Ph-overset(O)overset(||)(C)-NH_(2)+Ph-CH_(2)-overset(O)overset(||)(C)-overset(15)(N)H_(2) overset(overset ... (2)-NH_(2)` D. `Ph-overset(15)(N)H_(2)`

Description : Compound (A) `C_(12)H_(20)` discharges the colour of `Br_(2)-H_(2)O` and cold `KMnO_(4)` . On reduction with `H_(2)`/Pt it gives compound (B) `C_(12)H

Last Answer : Compound (A) `C_(12)H_(20)` discharges the colour of `Br_(2)-H_(2)O` and cold `KMnO_(4)` . On ... Find structure of A : A. B. C. D. None of these

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 : The oxidation state of Cr in `[Cr(H_(2)O)_(6)]Cl_(3), [Cr(C_(6)H_(6))_(2)], and K_(2)[Cr(CN)_(2)(O)_(2)(O_(2))(NH_(3))]` respectively are :

Last Answer : The oxidation state of Cr in `[Cr(H_(2)O)_(6)]Cl_(3), [Cr(C_(6)H_(6))_(2)], and K_(2)[Cr(CN)_(2)(O)_(2 ... and +4` C. `+3,+4 and +6` D. `+3,+2 and +4`

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