94420 + Interview Questions in Chemistry in Class 12

1.	Observe the following two reactions: (I). CH_(3)-underset(O)underset(\|\|)C-CH+C_(2)H_(5)overset(18)Hoverset(H_(2)SO_(4))to"products"+"water" (II). (X)+"water"overset(("sodium hydroxide")/(Delta))toCH_(3)-underset(O)underset(\|\|)(C)-overset(18)(O)Na+C_(2)H_(5)OH the correct statements are:
Answer» In reaction(I) the PRODUCTS is `CH_(3)-underset(O)underset(\|\|)C-overset(18)O-C_(2)H_(5)` In reaction (II) the REACTANT is `CH_(3)-underset(O)underset(\|\|)C-overset(18)C-C_(2)H_(5)` In reaction (II) the REAGENT is `(H_(2)overset(18))/(Naoverset(18)OH)` Reaction (I) is irreversible while reaction (II) is reversible. Solution :(i). (ii). `CH_(3)-underset(O)underset(\|\|)C-OC_(2)H_(5)+H_(2)overset(18)(C)` `underset("Basic medium")overset((Naoverset(18)(O)H)/(Delta))toCH_(3)-underset(O)underset(\|\|)C-overset(18)(O)Na` `+C_(2)H_(5)OH`

Discussion

2.	Observe the following statements? Bleaching powder is used in the preparation of Chloroform II. Bleaching powder decomposes in the presence of CoCl_(2) to liberate O_(2) III. Aqueoue KHF_(2) is used in the preparation of Fluorine.
Answer» I, II and III are correct Only II is correct Only I and III are correct Only I and II are correct. Solution :FUSED `KHF_(2)` USED in the preparation of flurionebut no AQ `KHF_(2)`

Discussion

3.	Observe the following statements (i) Silicon doped with P is a p-type semiconductor (ii) Presence of Schottky defects decreases the density (iii) Among simple cubic (sc), body centered cubic (bcc) and cubic close packing (ccp) stru ctu res, the p ack in g e fficie n cy is highest for ccp The correct statements are
Answer» I,II and III I and iii I and ii ii and iii ANSWER :D

Discussion

4.	Observe the following statements 1) Lanthanides actively participate in chemical reactions 2) The basic nature of hydroxides of lantha nides increases from La(OH)_3to Lu(OH)_3 3) Lanthanides do not form coordinate compounds as readily as d-block metals The correct statements are
Answer» 2 & 3 1,2 % 3 1 & 3 1 & 2 Answer :C

Discussion

5.	Observe the following sequence of reations P shows geometrical isomersm.Q gives positive Tollen's test and the oxidation product of Tollen's test followed by acidification is the strongest acid among its all position isomers. R gives positive lab tests with 2,4-DNP, Fehling solution and I_2//NaOH reagents. Identify the structure of R.
Answer» HCOOH `CH_3HO` `BrCH_2-CHO` `H-oversetoverset(O)(\|\|)C-Br` SOLUTION :

Discussion

6.	Observe the following sequence of reations P shows geometrical isomersm.Q gives positive Tollen's test and the oxidation product of Tollen's test followed by acidification is the strongest acid among its all position isomers. R gives positive lab tests with 2,4-DNP, Fehling solution and I_2//NaOH reagents. What could be the structure of Q ?
Answer» ANSWER :D

Discussion

7.	Observe the following sequence of reations P shows geometrical isomersm.Q gives positive Tollen's test and the oxidation product of Tollen's test followed by acidification is the strongest acid among its all position isomers. R gives positive lab tests with 2,4-DNP, Fehling solution and I_2//NaOH reagents. The compound P can be
Answer» ANSWER :B

Discussion

8.	Observe the following sequence of reactions P shows geometrical isomersm. Q gives positive Tollen's test and the oxidation product of Tollen's test followed by acidification is the strongest acis among its all position isomers. R gives positive lab test with 2,4,-DNP, Fehling solutioni and I_(2)//NaOH reagents. Identify the structure of R[GOC-POC]
Answer» `HCOOH`<BR>`CH_(3)CHO` `BrCH_(2)CHO` `H-overset(O)overset(\|\|)(C)-Br` Solution :NA

Discussion

9.	Observe the following sequence of reactions P shows geometrical isomersm. Q gives positive Tollen's test and the oxidation product of Tollen's test followed by acidification is the strongest acids among its all position isomers. R gives positive lab test with 2,4,-DNP, Fehling solution and I_(2)//NaOH reagents. The compound P can be
Answer» SOLUTION :NA

Discussion

10.	Observe the following sequence of reactions P shows geometrical isomers. Q gives positive Tollen's test and the oxidation product of Tollen's test followed by acidification is the strongest acis among its all position isomers. R gives positive lab test with 2,4,-DNP, Fehling solutioni and I_(2)//NaOH reagents. What could be the structure of Q? [GOC-POC]
Answer» SOLUTION :NA

Discussion

11.	Observe the following sequence of reaction and answer the questions based on it Phenylacetyleneoverset(CH_3MgBr)underset(-CH_4)toxunderset((ii)H^(o+))overset((i)CO_2)toyunderset(HgSO_4)overset(H_2O // H_2SO_4)tozoverset(Delta)tow Which of the following compound give benzoic acid on KMnO_4 oxidation
Answer» w y z all Solution :

Discussion

12.	Observe the following sequence of reaction and answer the questions based on it Phenylacetyleneoverset(CH_3MgBr)underset(-CH_4)toxunderset((ii)H^(o+))overset((i)CO_2)toyunderset(HgSO_4)overset(H_2O // H_2SO_4)tozoverset(Delta)tow Which of the following statement is not correct
Answer» y decolourises `Br_2//H_2O` solution on HEATING z `CO_2` is LIBERATED w on REACTION with NAOI gives yellow ppt x LIBERATES `H_2` gas with Na metal Solution :

Discussion

13.	Observe the following sequence of reaction and answer the questions based on it. Phenylacetylene overset(CH_(3)MgBr)underset(-CH_(4))to x overset((i)CO_(2))underset((ii)H^(o+))to y overset(H_(2)O //H_(2)SO_(4))underset(HgSO_(4))to z overset(Delta)to w Which of the following compound give benzoic acid on KMnO_(4) oxidation
Answer» w y z all SOLUTION :Any mono SUBSTITUTED benzene oxidise to BENZOIC acid.

Discussion

14.	Observe the following sequence of reaction and answer the questions based on it. Phenylacetylene overset(CH_(3)MgBr)underset(-CH_(4))to x overset((i)CO_(2))underset((ii)H^(o+))to y overset(H_(2)O //H_(2)SO_(4))underset(HgSO_(4))to z overset(Delta)to w Which of the following statement is not correct
Answer» y decolourises `Br_(2)//H_(2)O` solution z on heating liberates `CO_(2)` gas w on reaction with NAOL GIVES yellow ppt x liberates `H_(2)` gas with Na metal Solution :X is an anion and it has no acidic HYDROGEN

Discussion

15.	Observe the following sequence of reaction and answer the questions based on it. Phenylacetylene overset(CH_(3)MgBr)underset(-CH_(4))to x overset((i)CO_(2))underset((ii)H^(o+))to y overset(H_(2)O //H_(2)SO_(4))underset(HgSO_(4))to z overset(Delta)to w Compound z is
Answer» `Ph-CH_(2)-OVERSET(O)overset(\|\|)(C)-COOH` `Ph-overset(O)overset(\|\|)(C)-CH_(2)-COOH` `Ph-CH_(2)-COOH` Solution :Z is `Ph-overset(O)overset(\|\|)(C)-CH_(2)-COOH`

Discussion

16.	Observe the following reactions and its mechanistic steps and intermediate products. The leaving group of step (V) in reaction -2:
Answer» `CH_3COO^(THETA)` `CO_2` `PhCOO^(Theta)` `Ph-CH=CH-COOH` SOLUTION :

Discussion

17.	Observe the following sequence of reaction and answer the questions based on it Phenylacetyleneoverset(CH_3MgBr)underset(-CH_4)toxunderset((ii)H^(o+))overset((i)CO_2)toyunderset(HgSO_4)overset(H_2O // H_2SO_4)tozoverset(Delta)tow Compound z is
Answer» `Ph-CH_2-oversetoverset(O)(\|\|)C-COOH` `Ph-oversetoverset(O)(\|\|)C-CH_2-COOH` `Ph-CH_2-COOH` SOLUTION :

Discussion

18.	Observe the following reactions The reagent R_(1) and R_(2) can be respectively.
Answer» NaI/Acetone, aq. `AgNO_(3)` AQUEOUS KOH, HI aq. `AgNO_(3)`, NaI/Acetone HI, aqueous KOH Answer :D

Discussion

19.	Observe the following reactions (I)to (IV) and answer questions Z and W are
Answer» IDENTICAL compounds Diastereomers Structural isomers Homologues Solution :

Discussion

20.	Observe the following reactions (I)to (IV) and answer questions X and Y are
Answer» POSITIONAL isomers Geometrical isomers Identical compounds Optical isomers Solution :

Discussion

21.	Observe the following reactions and its mechanistic steps and intermediate products. If Ph-CH=O^(18) is used then O^18 is traced inreaction-2:
Answer» `Ph-undersetunderset(O)(\|\|)C-O^(18)-H` `CH_3-undersetunderset(O)(\|\|)C-C^(18)-H` `Ph-CH=CH-undersetunderset(O)(\|\|)C-O^(18)-H` `H-O-undersetunderset(O)(\|\|)C-O^(18)-H` SOLUTION :

Discussion

22.	Observe the following reactions and its mechanistic steps and intermediate products. The intermediate product similar to (IV) following in the reaction-(2):
Answer» SOLUTION :

Discussion

23.	Observe the following reactions and answer the following questions The product T is
Answer» ANSWER :B

Discussion

24.	Observe the following reactions and answer the following questions The product mixture 'V' does not have.
Answer» SOLUTION :

Discussion

25.	Observe the following reaction sequence X can be
Answer» SOLUTION :

Discussion

26.	Observe the following reaction : Which of the following is/are incorrect order of acid strength :
Answer» SOLUTION : Since a strong acid DISPLACES a WEAK acid from its SALT and FORMS its own salt.

Discussion

27.	Observe the following reaction sequence carefully.Find the total number of stereoisomers formed in step (6)
Answer» SOLUTION :

Discussion

28.	Observe the following reaction sequence Answer the following question in the given format: P=Number of organic products formed in step-1 Q=Number of organic products formed in step-2 (singnificant products) R=Number of organic products formed in step-3 (singnificant products) S=In which step aromatic electrophilic substitution has taken place
Answer» SOLUTION :

Discussion

29.	Observe the following reaction and mention the number which show slowest and rate determine step.
Answer» Solution :In free radical SUBSTITUTION REACTION alkyl free radical formation is RATE DETERMINING step.

Discussion

30.	Observe the following reaction and mark the correct statement given below-
Answer» METHYL glucosides do not react with Fehling's or Tollen's reagent The REACTION PASSES through a carbocation The two forms of glucosides are enantiomers The non-reducing CHARACTER of glucoside indicates the absence of free-CHO group in it. Solution :Methyl glycosides can't reduce fehling and Tollen's reagent DUE to absence of free C = O group.

Discussion

31.	Observe the following reaction and find out that how many number of reactant stereoisomers can be reduced to optically inactive meso products.
Answer» SOLUTION :

Discussion

32.	Observe the following reaction and determine True statement
Answer» If aromatic RING I have `-NO_(2)` group then RATE of REACTION will decrease. If aromatic ring II have `-NO_(2)` group then rate of reaction will increase. In this reaction Wheland intermediate will form. In this reaction Meisenheimer intermediate is formed. Solution :It is coupling reaction.

Discussion

33.	Observe the following reaction, 2A+B rarr C The rate of formation of C is 2.2xx10^(-3)" M m in"^(-1). What is the value of -(d[A])/(dt) ("in moL"^(-1)" m in "^(-1)) ?
Answer» `2.2xx10^(-3)` `1.1xx10^(-3)` `4.4xx10^(-3)` `5.5xx10^(-3)` SOLUTION :`2A + B rarr C` `(d[C])/(dt)=(1)/(2) ((-d[A])/(dt)) rArr (-d[A])/(dt) =4.4xx10^(-3)`

Discussion

34.	Observe the following reaction A_((g))+3B_((g))to2C_((g))The rate of this reaction -(d[A])/("d t") is 3xx0^(-3)"mol. lit"^(-1)."min"^(-1). What is the value of -(d[B])/("d t") in "mol. lit"^(-1)."min"^(-1) ?
Answer» `3xx10^(-3)` `9XX10^(-3)` `10^(-3)` `1.5xx10^(-3)` Answer :B

Discussion

35.	Observe the following reaction:2A + B to C The rate of formation of C is 2.2xx10^(3) mol L^(-1) min^(-1).What is the value - (d(A))/(dt) ("in "mol L^(-1) mi n^(-1))
Answer» `2.2xx10^(-3)` `1.1xx10^(-3)` `4.4xx10^(-3)` `5.5xx10^(-3)` ANSWER :C

Discussion

36.	Observe the following flow chart and write the sum of the number of x,y, z.
Answer» SOLUTION :

Discussion

37.	Observe the following feasible reaction: Q. Which of the following is the correct order of acidic strength:
Answer» None Answer :A

Discussion

38.	Observe the following feasible reaction: Q. Identify the feasible reactions
Answer» ANSWER :A::D

Discussion

39.	Observe the following feasible reaction: Q. Which of the following compound does not react with NaHCO_(3).
Answer» ANSWER :A

Discussion

40.	Observe the following experiment
Answer» SOLUTION :

Discussion

41.	Observe the following data regarding {:(""2NH_(3)overset(W)(to)N_(2)+3H_(2)),("Pressure (in atm) " :"51020"),("Half life (min)" : "3.61.80.9"):} The unit of K is
Answer» `"min"^(-1)` `"ATM - min"^(-1)` `"(atm - min)"^(-1)` `"atm"^(-2) - "min"^(-1)` ANSWER :B

Discussion

42.	Observe the following compounds Number of coumpound which can gives positive Haloform test = (x) Number of compound which can gives positive Lucas reagent test = (y) Report your answer (x+y)
Answer» Solution :Compound `(I), (IV), (V), (VII)` and `(IX)` gives positive haloform compound `(III), (VII)` and `(IX)` gives positive Lucas REAGENT, `x = 5, y = 3` so, `(5+3) = 8`.

Discussion

43.	Observe the following compound and write the number of hydrogen atom involved in hyper conjugation (with carbocation)?
Answer» Solution : TOTAL NUMBER of HYDROGEN involved in HYPERCONJUGATION with CARBOCATION =6

Discussion

44.	Observe the following compound and select +ve & -ve test respectively.
Answer» `+ + + -` `+ + + +` `+ - + -` `+ - - +` SOLUTION :

Discussion

45.	Observe the following abbrevations pi_(obs) = observed colligative property assuming normal behaviour of solute. Van't Haff factor (i) is given by
Answer» `i=pi_(OBS)XX pi_(CAL)` `i=pi_(obs)+pi_(cal)` `i=pi_(obs)-pi_(cal)` `i=(pi_(obs))/(pi_(cal))` ANSWER :D

Discussion

46.	Observe the esterification mechanisms for primary and teriary alcohols. CH_(3)-COOH+C_(2)H_(5)overset(18)(O)H overset(Conc. H_(2)SO_(4))to(P) CH_(3)-COOH+(CH_(3))_3C-overset(18)(O)H overset(Conc. H_(2)SO_(4))to (Q) In the above reaction (P) and (Q) are respectively
Answer» `CH_(3)- overset(O)overset(\|\|)(C)-O-C_(2)H_(5),CH_3-overset(O)overset(\|\|)(C)-overset(18)(O)-overset(CH_(3))overset(\|)UNDERSET(CH_(3))underset(\|)(CH)_(3)-CH_(3)` `CH_(3)-overset(O)overset(\|\|)(C)-overset(18)(O)-C_(2)H_(5),CH_(3)-overset(O)overset(\|\|)(C)-O-underset(CH_(3))underset(\|)underset(CH_(3))underset(\|)(C)-CH_(3)` `C_(2)H_(5)-overset(O)overset(\|\|)(C)-overset(18)(O)-CH_(3),CH_(3)-overset(O)overset(\|\|)(C)-O-underset(CH_(3))underset(\|)overset(CH_(3))overset(\|)(C)-CH_(3)` `CH_(3)-overset(O)overset(\|\|)(C)-overset(18)(O)-C_(2)H_(5),CH_(3)-overset(O)overset(\|\|)(C)-overset(18)(O)-underset(CH_(3))underset(\|)overset(CH_(3))overset(\|)(C)-CH_(3)` SOLUTION :

Discussion

47.	Observe the esterification mechanisms for primary and teriary alcohols. (+) Octan -2-ol esterifies with Acetic acid to give optically inactive racemised product. It must have gone by
Answer» TYPE I mechanism Type II mechanism Mix type I and type II mechanism more by type I and less by type II mechanism Solution :Since (+) Octan -2-ol racemises on reaction with acetic ACID, therefore it MUST have GONE through an `S_(N)1` reaction i.e., type II reaction

Discussion

48.	Observe the esterfication mechanisms for primary and tertiary alcohols. CH_3-COOH+Ph-undersetunderset(C_2H_5)(\|)oversetoverset(CH_3)(\|)C-OHoverset(Conc.H_2SO_4)to(Y)
Answer» (X) is optically ACTIVE while (Y) is optically INACTIVE Both (X) and (Y) are optically active Both (X) and (Y) are optically inactive (X) is optically inactive while (Y) is optically active Solution :X is formed by type-1 MECHANISM hence CONFIGURATION is retained. Y is formed by type-2 mechanism hence recemic product is OBTAINED.

Discussion

49.	Observe the esterfication mechanisms for primary and tertiary alcohols. CH_3-COOH+C_2H_6overset(18)OHoverset(Conc.H_2SO_4)to(P) CH_3-COOH+(CH_3)_3C-overset(18)OHoverset(Conc.H_2SO_4)(Q) In the above reaction (P) and (Q) are respectively :
Answer» <P>`CH_3-oversetoverset(O)(\|\|)C-O-C_2H_6,CH_3-oversetoverset(O)(\|\|)C-overset(18)(O)-undersetunderset(CH_3)(\|)oversetoverset(CH_3)(\|)C-CH_3` `CH_3-oversetoverset(O)(\|\|)C-overset(18)(O)-C_2H_5,CH_3-oversetoverset(O)(\|\|)C-O-undersetunderset(CH_3)(\|)oversetoverset(CH_3)(\|)C-CH_3` `C_2H_5-oversetoverset(O)(\|\|)C-overset(18)(O)-CH_3, CH_3-oversetoverset(O)(\|\|)C-O-undersetunderset(CH_3)(\|)oversetoverset(CH_3)(\|)C-CH_3` `CH_3-oversetoverset(O)(\|\|)overset(18)(O)-C_2H_6,CH_3-oversetoverset(O)(\|\|)C-overset(18)(O)-undersetunderset(CH_3)(\|)oversetoverset(CH_3)(\|)C-CH_3` Solution :P is formed by type-1 MECHANISM and Q is formed by type-2 mechanism.

Discussion

50.	Observe the esterfication mechanisms for primary and tertiary alcohols. (+) Octan-2-ol esterifies with Acetic acid to give optically inactive recemised product.It must have gone by
Answer» TYPE I MECHANISM Type II mechanism Mix type I and type II mechanism More by type I and LESS by type II mechanism Solution :Octan-2-ol is `2^@` alcohol, it forms ESTER by type -1 mechanism

Discussion

Explore topic-wise InterviewSolutions in Current Affairs.

Observe the following two reactions: (I). CH_(3)-underset(O)underset(||)C-CH+C_(2)H_(5)overset(18)Hoverset(H_(2)SO_(4))to"products"+"water" (II). (X)+"water"overset(("sodium hydroxide")/(Delta))toCH_(3)-underset(O)underset(||)(C)-overset(18)(O)Na+C_(2)H_(5)OH the correct statements are:

Observe the following statements? Bleaching powder is used in the preparation of Chloroform II. Bleaching powder decomposes in the presence of CoCl_(2) to liberate O_(2) III. Aqueoue KHF_(2) is used in the preparation of Fluorine.

Observe the following statements 1) Lanthanides actively participate in chemical reactions 2) The basic nature of hydroxides of lantha nides increases from La(OH)_3to Lu(OH)_3 3) Lanthanides do not form coordinate compounds as readily as d-block metals The correct statements are

Observe the following sequence of reaction and answer the questions based on it Phenylacetyleneoverset(CH_3MgBr)underset(-CH_4)toxunderset((ii)H^(o+))overset((i)CO_2)toyunderset(HgSO_4)overset(H_2O // H_2SO_4)tozoverset(Delta)tow Which of the following compound give benzoic acid on KMnO_4 oxidation

Observe the following sequence of reaction and answer the questions based on it Phenylacetyleneoverset(CH_3MgBr)underset(-CH_4)toxunderset((ii)H^(o+))overset((i)CO_2)toyunderset(HgSO_4)overset(H_2O // H_2SO_4)tozoverset(Delta)tow Which of the following statement is not correct

Observe the following sequence of reaction and answer the questions based on it. Phenylacetylene overset(CH_(3)MgBr)underset(-CH_(4))to x overset((i)CO_(2))underset((ii)H^(o+))to y overset(H_(2)O //H_(2)SO_(4))underset(HgSO_(4))to z overset(Delta)to w Which of the following statement is not correct

Observe the following sequence of reaction and answer the questions based on it. Phenylacetylene overset(CH_(3)MgBr)underset(-CH_(4))to x overset((i)CO_(2))underset((ii)H^(o+))to y overset(H_(2)O //H_(2)SO_(4))underset(HgSO_(4))to z overset(Delta)to w Compound z is

Observe the following reactions and its mechanistic steps and intermediate products. The leaving group of step (V) in reaction -2:

Observe the following sequence of reaction and answer the questions based on it Phenylacetyleneoverset(CH_3MgBr)underset(-CH_4)toxunderset((ii)H^(o+))overset((i)CO_2)toyunderset(HgSO_4)overset(H_2O // H_2SO_4)tozoverset(Delta)tow Compound z is

Observe the following reactions The reagent R_(1) and R_(2) can be respectively.

Observe the following reactions (I)to (IV) and answer questions Z and W are

Observe the following reactions (I)to (IV) and answer questions X and Y are

Observe the following reactions and its mechanistic steps and intermediate products. If Ph-CH=O^(18) is used then O^18 is traced inreaction-2:

Observe the following reactions and its mechanistic steps and intermediate products. The intermediate product similar to (IV) following in the reaction-(2):

Observe the following reactions and answer the following questions The product T is

Observe the following reactions and answer the following questions The product mixture 'V' does not have.

Observe the following reaction sequence X can be

Observe the following reaction : Which of the following is/are incorrect order of acid strength :

Observe the following reaction sequence carefully.Find the total number of stereoisomers formed in step (6)

Observe the following reaction and mention the number which show slowest and rate determine step.

Observe the following reaction and mark the correct statement given below-

Observe the following reaction and find out that how many number of reactant stereoisomers can be reduced to optically inactive meso products.

Observe the following reaction and determine True statement

Observe the following reaction, 2A+B rarr C The rate of formation of C is 2.2xx10^(-3)" M m in"^(-1). What is the value of -(d[A])/(dt) ("in moL"^(-1)" m in "^(-1)) ?

Observe the following reaction A_((g))+3B_((g))to2C_((g))The rate of this reaction -(d[A])/("d t") is 3xx0^(-3)"mol. lit"^(-1)."min"^(-1). What is the value of -(d[B])/("d t") in "mol. lit"^(-1)."min"^(-1) ?

Observe the following reaction:2A + B to C The rate of formation of C is 2.2xx10^(3) mol L^(-1) min^(-1).What is the value - (d(A))/(dt) ("in "mol L^(-1) mi n^(-1))

Observe the following flow chart and write the sum of the number of x,y, z.

Observe the following feasible reaction: Q. Which of the following is the correct order of acidic strength:

Observe the following feasible reaction: Q. Identify the feasible reactions

Observe the following feasible reaction: Q. Which of the following compound does not react with NaHCO_(3).

Observe the following experiment

Observe the following data regarding {:(""2NH_(3)overset(W)(to)N_(2)+3H_(2)),("Pressure (in atm) " :"51020"),("Half life (min)" : "3.61.80.9"):} The unit of K is

Observe the following compounds Number of coumpound which can gives positive Haloform test = (x) Number of compound which can gives positive Lucas reagent test = (y) Report your answer (x+y)

Observe the following compound and write the number of hydrogen atom involved in hyper conjugation (with carbocation)?

Observe the following compound and select +ve & -ve test respectively.

Observe the following abbrevations pi_(obs) = observed colligative property assuming normal behaviour of solute. Van't Haff factor (i) is given by

Observe the esterification mechanisms for primary and teriary alcohols. CH_(3)-COOH+C_(2)H_(5)overset(18)(O)H overset(Conc. H_(2)SO_(4))to(P) CH_(3)-COOH+(CH_(3))_3C-overset(18)(O)H overset(Conc. H_(2)SO_(4))to (Q) In the above reaction (P) and (Q) are respectively

Observe the esterification mechanisms for primary and teriary alcohols. (+) Octan -2-ol esterifies with Acetic acid to give optically inactive racemised product. It must have gone by

Observe the esterfication mechanisms for primary and tertiary alcohols. CH_3-COOH+Ph-undersetunderset(C_2H_5)(|)oversetoverset(CH_3)(|)C-OHoverset(Conc.H_2SO_4)to(Y)

Observe the esterfication mechanisms for primary and tertiary alcohols. CH_3-COOH+C_2H_6overset(18)OHoverset(Conc.H_2SO_4)to(P) CH_3-COOH+(CH_3)_3C-overset(18)OHoverset(Conc.H_2SO_4)(Q) In the above reaction (P) and (Q) are respectively :

Observe the esterfication mechanisms for primary and tertiary alcohols. (+) Octan-2-ol esterifies with Acetic acid to give optically inactive recemised product.It must have gone by