Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

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Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

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Description : Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

Last Answer : Arrange the following compounds in decreasing order of nucleophilic addition with semicarbazide `NH_(2)NHCONH_(2)` i.e., `ddot(N)H_(2)-ddot(Z)`

Description : Arrange the following carboxyl compounds in increasing order of their reactivity in nucleophilic addition reactions. Explain with proper reasoning : Benzaldehyde. p-tolualdeyde, p-nitrobenzaldehyde, Acetophenone.

Last Answer : Ans. Acetophenone is a ketone while all others are aldehydes, therefore it is least reactive. In p-tolualdehyde, there is methyl group (CH3 ) at para position w.r.t. to the ... overall order of increasing reactivity : acetophenone < p-tolualdehyde < benzaldehyde < p-nitrobenzaldehyde. 

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 : 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`

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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)`

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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 compounds in decreasing orders of rate of hydration. `(X) C Cl_(3)CHO " " (Y) CH_(3)CHO " " (Z)CH_(3)COCH_(3) " " (W) CF_(3)CHO`

Last Answer : Arrange the following compounds in decreasing orders of rate of hydration. `(X) C Cl_(3)CHO ... . WgtZgtXgtY B. WgtXgtYgtZ C. WgtYgtZgtX D. WgtZgtYgtX

Description : Arrange the following compounds in decreasing orders of rate of hydration. `(X) C Cl_(3)CHO " " (Y) CH_(3)CHO " " (Z)CH_(3)COCH_(3) " " (W) CF_(3)CHO`

Last Answer : Arrange the following compounds in decreasing orders of rate of hydration. `(X) C Cl_(3)CHO ... . WgtZgtXgtY B. WgtXgtYgtZ C. WgtYgtZgtX D. WgtZgtYgtX

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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`

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Last Answer : Arrange the following carbanions in decreasing orde of stability: `HC-=bar(C)(I)," "H_(3 ... `IIgtIgtIIIgtIV` C. `IVgtIIIgtIIgtI` D. `IgtIIgtIIIgtIV`

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 in the decreasing order of Vander Waal’s radii: Cl, H, O, N.

Last Answer : Ans.The overall decreasing order is: Cl> N > O >H.

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 : 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 : The decreasing order of strength of the bases, `OH^(-), NH_(2)^(-), H-C-=C^(-)` and `CH_(3)-CH_(2)^(-)`:

Last Answer : The decreasing order of strength of the bases, `OH^(-), NH_(2)^(-), H-C-=C^(-)` and `CH_(3)-CH_(2)^(-)`: ... " IV"` D. `"II "gt" III "gt" I "gt" IV"`

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

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Description : Arrange the following in decreasing order of rate of nitration :-

Last Answer : Arrange the following in decreasing order of rate of nitration :- A. `b gt a = c gt d` B. `d gt a = c gt b` ... gt a gt c gt d` D. `a gt c gt d gt b`

Description : Arrange the following in decreasing order of acidic strength:

Last Answer : Arrange the following in decreasing order of acidic strength: A. `I gt II gt III gt IV` B. `IV gt III gt II ... III gt I` D. `IV gt II gt III gt I`

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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`

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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

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Last Answer : Ans: (b)

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Last Answer : (A) Jaw crusher, Ball mill, Fluid energy mill

Description : Arrange the following in order of decreasing reactivity towards alkanes. HCl, HBr, HI, HF

Last Answer : Ans. HI> HBr> HCl >HF

Description : Arrange the first group elements in the decreasing order of Hydration Enthalpy 

Last Answer : The hydration enthalpies of alkali metal ions decrease with increase in ionic sizes. Li+ > Na+ > K+ > Rb+ > Cs+

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Last Answer : `{:(,"Compounds",,"O.N."),((A),KMn^(**)O_(4),(1),+4),((B),Ni^(**)(CO)_(4),(2),+7),((C),[Pt^(**)(NH_(3) ... ),(2,3,1,4):}` D. `{:(A,B,C,D),(4,1,2,3):}`

Description : Which of the following is an example of nucleophilic addition of acetone?

Last Answer : Which of the following is an example of nucleophilic addition of acetone? A. Ketal formation B ... gas C. Cyanohydrin formation D. Bisulphite additon

Description : Which gives nucleophilic addition reaction?

Last Answer : Which gives nucleophilic addition reaction? A. Methanal B. Ethanal C. Propanone D. Propene

Description : Nucleophilic addition reaction will be most favoured in

Last Answer : Nucleophilic addition reaction will be most favoured in A. `CH_(3)CH_(2)CHO` B. `CH_(3)CHO` C. `CH_(3)CH_(2)CH_(2 ... |)C-CH_(3)` D. `(CH_(3))_(2)C=O`

Description : What is nucleophilic addition reaction ?

Last Answer : When the attacking species during the addition reaction is Nucleophilic, it is nucleophilic addition reaction. Ex; Acetaldehyde cynohydrin

Description : Benzene reacts with concentrated HNO3 in the presence of concentrated H2SO4 to give nitrobenzene. This reaction is an example of (a) Electrophilic addition (b) Nucleophilic addition (c) Electrophilic substitution (d) Nucleophilic substitution

Last Answer : Electrophilic substitution

Description : Benzene reacts with concentrated HNO3 in the presence of concentrated H2SO4 to give nitrobenzene. This reaction is an example of (a) Electrophilic addition (b) Nucleophilic addition (c) Electrophilic substitution (d) Nucleophilic substitution

Last Answer : Electrophilic substitution

Description : The characteristic reaction of carboxylic acids is : (a) electrophilic addition (b) electrophilic substitution (c) nucleophilic addition (d) nucleophilic substitution

Last Answer : nucleophilic substitution

Description : Why do aldehydes undergo nucleophilic addition reactions while esters undergo nucleophilic acyl substitution reactions? (a) The carbonyl carbon of an ester is more electrophilic than that of an aldehyde. (b) ... adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic

Last Answer : Once the nucleophile adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic

Description : Which of the following characterizes the reactions of aldehydes and ketones? (a) electrophilic addition (b) electrophilic substitution (c) nucleophilic acyl substitution (d) nucleophilic addition; free radical addition

Last Answer : nucleophilic addition; free radical addition

Description : Acetone reacts with HCN to form a cyanohydrin. It is an example of (a) Electrophilic addition (b) Electrophilic substitution (c) Nucleophilic addition (d) Nucleophilic substitution

Last Answer : Nucleophilic addition

Description : Alkyl halides undergo (a) Electrophilic substitution reactions (b) Electrophilic addition reactions (c) Nucleophilic substitution reactions (d) Nucleophilic addition reactions

Last Answer : Nucleophilic substitution reactions

Description : Propene reacts with bromine to form 1,2-dibromopropane. This is an example of (a) Nucleophilic addition (b) Electrophilic addition (c) Nucleophilic substitution (d) Electrophilic substitution

Last Answer : Electrophilic addition

Description : The chlorination of methane to give CCl4 is an example of (a) an electrophilic addition (b) a free-radical substitution (c) a nucleophilic addition (d) an electrophilic substitution

Last Answer : a free-radical substitution

Description : Among the given compounds, the most susceptible to nucleophilic attack at the cabonyl group is:

Last Answer : Among the given compounds, the most susceptible to nucleophilic attack at the cabonyl group is: A. `MeCOCl` B. `MeCHO` C. `MeCOOMe` D. `MeCOOCOMe`

Description : Which is decreasing order of acidity in, `HCOOH(I), CH_(3)COOH(II), CH_(3)CH_(2)COOH(III) and C_(6)H_(5)COOH(IV)`?

Last Answer : Which is decreasing order of acidity in, `HCOOH(I), CH_(3)COOH(II), CH_(3)CH_(2)COOH( ... B. `IVgtIIIgtIIgtI` C. `IVgtIgtIIgtIII` D. `IgtIVgtIIgtIII`

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 : Arrange the following compounds in increasing order of their acid strength. Benzoic acid, 4-Nitrobenzoic acid, 3, 4-dinitrobenzoic acid, 4-methoxy benzoic acid.

Last Answer : Since electron donating gps. decrease the acid strength therefore 4-methoxybenzoic acid is a weaker acid because methoxy sp. is E. D. G. than benzoic acid. Further since electron withdrawing gps. increase ... : 4-methoxybenzoic acid < benzoic acid < 4-nitrobenzoic acid < 3, 4, dinitrobenzoic acid.

Description : Which is the correct order of decreasing acidity in the following compounds? A. H2O B. CH3CH3 C. NH3 D. CH2=CH2 E. HC≡CH (a) A > E > C > D > B (b) A > E > D > B > C (c) E > A > C > B > D (d) A > C > E > D > B

Last Answer : A > E > C > D > B

Description : When semicarbazide reacts with a ketone (or aldehyde) to form semicarbazone. Only one nitrogen atom of semicarbazide acts as a nucleophile and attack

Last Answer : When semicarbazide reacts with a ketone (or aldehyde) to form semicarbazone. Only one ... atoms of semicarbazide are relatively non nucleophilic ?