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Strong reducing behaviour of \[\ce{H3PO2}\] is due to ______.
Concept: undefined >> undefined
Which of the following statements are correct?
(i) \[\ce{CaF2 + H2SO4 -> CaSO4 + 2HF}\]
(ii) \[\ce{2HI + H2SO4 -> I2 + SO2 + 2H2O}\]
(iii) \[\ce{Cu + 2H2SO4 -> CuSO4 + SO2 + 2H2O}\]
(iv) \[\ce{Nacl + H2SO4 -> NaHSO4 + HCl}\]
Concept: undefined >> undefined
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Write a balanced chemical equation for the reaction showing catalytic oxidation of NH3 by atmospheric oxygen.
Concept: undefined >> undefined
Out of \[\ce{H2O}\] and \[\ce{H2S}\], which one has higher bond angle and why?
Concept: undefined >> undefined
Using valence bond theory, explain the following in relation to the complexes given below:
\[\ce{[Mn(CN)6]^{3-}}\]
(i) Type of hybridisation.
(ii) Inner or outer orbital complex.
(iii) Magnetic behaviour.
(iv) Spin only magnetic moment value.
Concept: undefined >> undefined
Using valence bond theory, explain the following in relation to the complexes given below:
\[\ce{[Co(NH3)6]^{3+}}\]
(i) Type of hybridisation.
(ii) Inner or outer orbital complex.
(iii) Magnetic behaviour.
(iv) Spin only magnetic moment value.
Concept: undefined >> undefined
Using valence bond theory, explain the following in relation to the complexes given below:
\[\ce{[Cr(H2O)6]^{3+}}\]
(i) Type of hybridisation.
(ii) Inner or outer orbital complex.
(iii) Magnetic behaviour.
(iv) Spin only magnetic moment value.
Concept: undefined >> undefined
Using valence bond theory, explain the following in relation to the complexes given below:
\[\ce{[FeCl6]^{4-}}\]
(i) Type of hybridisation.
(ii) Inner or outer orbital complex.
(iii) Magnetic behaviour.
(iv) Spin only magnetic moment value.
Concept: undefined >> undefined
Which of the following compounds will give racemic mixture on nucleophilic substitution by \[\ce{OH-}\] ion?
(a) \[\begin{array}{cc}
\phantom{}\ce{CH3 - CH - Br}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
(b) \[\begin{array}{cc}
\phantom{..}\ce{Br}\\
\phantom{}|\\
\phantom{}\ce{CH3 - C - CH3}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
(c) \[\begin{array}{cc}
\phantom{....}\ce{CH3 - CH - CH2Br}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
Concept: undefined >> undefined
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
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| (c) | ![]() |
Concept: undefined >> undefined
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
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| (b) | ![]() |
| (c) | ![]() |
Concept: undefined >> undefined
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
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| (b) | ![]() |
| (c) | ![]() |
Concept: undefined >> undefined
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
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| (b) | ![]() |
| (c) | ![]() |
Concept: undefined >> undefined
Haloarenes are less reactive than haloalkanes and haloalkenes. Explain.
Concept: undefined >> undefined
Allyl chloride is hydrolysed more readily than n-propyl chloride. Why?
Concept: undefined >> undefined
Phenol is less acidic than ______.
Concept: undefined >> undefined
Phenol can be distinguished from ethanol by the reactions with:
(i) \[\ce{Br2/water}\]
(ii) \[\ce{Na}\]
(iii) Neutral \[\ce{FeCl3}\]
(iv) All the above
Concept: undefined >> undefined
Write the IUPAC name of the following compound.
\[\begin{array}{cc}
\phantom{.}\ce{CH3 - CH - CH - CH - CH - CH3}\phantom{}\\
\phantom{......}|\phantom{......}|\phantom{......}|\phantom{.....}|\phantom{........}\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{C2H5}\phantom{.}\ce{OH}\phantom{...}\end{array}\]
Concept: undefined >> undefined
What is denatured alcohol?
Concept: undefined >> undefined
Out of 2-chloroethanol and ethanol which is more acidic and why?
Concept: undefined >> undefined












