Please select a subject first
Advertisements
Advertisements
Match the species in Column I with the bond order in Column II.
| Column I | Column II |
| (i) \[\ce{NO}\] | (a) 1.5 |
| (ii) \[\ce{CO}\] | (b) 2.0 |
| (iii) \[\ce{O^{-}2}\] | (c) 2.5 |
| (iv) \[\ce{O2}\] | (d) 3.0 |
Concept: undefined >> undefined
Which of the following pair is expected to have the same bond order?
Concept: undefined >> undefined
Advertisements
As the temperature increases, average kinetic energy of molecules increases. What would be the effect of increase of temperature on pressure provided the volume is constant?
Concept: undefined >> undefined
Match the graphs between the following variables with their names:
| Graphs | Names | ||
| (i) | Pressure vs temperature graph at constant molar volume. | (a) | Isotherms |
| (ii) | Pressure vs volume graph at constant temperature. | (b) | Constant temperature curve |
| (iii) | Volume vs temperature graph at constant pressure. | (c) | Isochores |
| (d) | Isobars |
Concept: undefined >> undefined
Assertion (A): The temperature at which vapour pressure of a liquid is equal to the external pressure is called boiling temperature.
Reason (R): At high altitude atmospheric pressure is high.
Concept: undefined >> undefined
How can production of hydrogen from water gas be increased by using water gas shift reaction?
Concept: undefined >> undefined
In which of the following, functional group isomerism is not possible?
Concept: undefined >> undefined
Which of the following pairs are position isomers?
| I. | \[\begin{array}{cc} \phantom{.......................}\ce{O}\\ \phantom{.......................}||\\ \ce{CH3 - CH2 - CH2 - CH2 - C - H} \end{array}\] |
| II. | \[\begin{array}{cc} \phantom{.................}\ce{O}\\ \phantom{.................}||\\ \ce{CH3 - CH2 - CH2 - C - H} \end{array}\] |
| III. | \[\begin{array}{cc} \ce{CH3 - CH2 - C - CH2 - CH3}\\ \phantom{}||\\ \phantom{}\ce{O} \end{array}\] |
| IV. | \[\begin{array}{cc} \ce{CH3 - CH - CH2 - C - H}\\ \phantom{...}|\phantom{............}||\phantom{}\\ \phantom{...}\ce{CH3}\phantom{.........}\ce{O}\phantom{} \end{array}\] |
(i) I and II
(ii) II and III
(iii) II and IV
(iv) III and IV
Concept: undefined >> undefined
Electrophiles are electron seeking species. Which of the following groups contain only electrophiles?
(i) \[\ce{BF3, NH3, H2O}\]
(ii) \[\ce{AlCl3, SO3, NO^{+}2}\]
(iii) \[\ce{NO^{+}2, CH^{+}3, CH3 - \overset{+}{C} = O}\]
(iv) \[\ce{C2H^{-}5, \overset{\bullet}{C2}H5, C2H^{+}5}\]
Concept: undefined >> undefined
Which of the following pairs are not functional group isomers?
| I. | \[\begin{array}{cc} \phantom{.......................}\ce{O}\\ \phantom{.......................}||\\ \ce{CH3 - CH2 - CH2 - CH2 - C - H} \end{array}\] |
| II. | \[\begin{array}{cc} \phantom{.................}\ce{O}\\ \phantom{.................}||\\ \ce{CH3 - CH2 - CH2 - C - H} \end{array}\] |
| III. | \[\begin{array}{cc} \ce{CH3 - CH2 - C - CH2 - CH3}\\ \phantom{}||\\ \phantom{}\ce{O} \end{array}\] |
| IV. | \[\begin{array}{cc} \ce{CH3 - CH - CH2 - C - H}\\ \phantom{...}|\phantom{............}||\phantom{}\\ \phantom{...}\ce{CH3}\phantom{.........}\ce{O}\phantom{} \end{array}\] |
(i) II and III
(ii) II and IV
(iii) I and IV
(iv) I and II
Concept: undefined >> undefined
Nucleophile is a species that should have:
(i) A pair of electrons to donate
(ii) Positive charge
(iii) Negative charge
(iv) Electron-deficient species
Concept: undefined >> undefined
Consider structures I to VII and answer the question:
| I. | CH3 – CH2 – CH2 – CH2 – OH |
| II. | \[\begin{array}{cc} \ce{CH3 - CH2 - CH - CH3}\\ \phantom{.....}|\\ \phantom{.......}\ce{OH} \end{array}\] |
| III. | \[\begin{array}{cc} \phantom{...}\ce{CH3}\\ \phantom{}|\\ \ce{CH3 - C - CH3}\\ \phantom{}|\\ \phantom{..}\ce{OH} \end{array}\] |
| IV. | \[\begin{array}{cc} \ce{CH3 - CH - CH2 - OH}\\ |\phantom{........}\\ \ce{CH3}\phantom{......} \end{array}\] |
| V. | CH3 – CH2 – O – CH2 – CH3 |
| VI. | CH3 – O – CH2 – CH2 – CH3 |
| VII. | \[\begin{array}{cc} \ce{CH3 - O - CH - CH3}\\ \phantom{...}|\\ \phantom{......}\ce{CH3} \end{array}\] |
Identify the pairs of compounds which are functional group isomers.
Concept: undefined >> undefined
Consider structures I to VII and answer the question:
| I. | CH3 – CH2 – CH2 – CH2 – OH |
| II. | \[\begin{array}{cc} \ce{CH3 - CH2 - CH - CH3}\\ \phantom{.....}|\\ \phantom{.......}\ce{OH} \end{array}\] |
| III. | \[\begin{array}{cc} \phantom{...}\ce{CH3}\\ \phantom{}|\\ \ce{CH3 - C - CH3}\\ \phantom{}|\\ \phantom{..}\ce{OH} \end{array}\] |
| IV. | \[\begin{array}{cc} \ce{CH3 - CH - CH2 - OH}\\ |\phantom{........}\\ \ce{CH3}\phantom{......} \end{array}\] |
| V. | CH3 – CH2 – O – CH2 – CH3 |
| VI. | CH3 – O – CH2 – CH2 – CH3 |
| VII. | \[\begin{array}{cc} \ce{CH3 - O - CH - CH3}\\ \phantom{...}|\\ \phantom{......}\ce{CH3} \end{array}\] |
Identify the pairs of compounds that represents position isomerism.
Concept: undefined >> undefined
Consider structures I to VII and answer the question:
| I. | CH3 – CH2 – CH2 – CH2 – OH |
| II. | \[\begin{array}{cc} \ce{CH3 - CH2 - CH - CH3}\\ \phantom{.....}|\\ \phantom{.......}\ce{OH} \end{array}\] |
| III. | \[\begin{array}{cc} \phantom{...}\ce{CH3}\\ \phantom{}|\\ \ce{CH3 - C - CH3}\\ \phantom{}|\\ \phantom{..}\ce{OH} \end{array}\] |
| IV. | \[\begin{array}{cc} \ce{CH3 - CH - CH2 - OH}\\ |\phantom{........}\\ \ce{CH3}\phantom{......} \end{array}\] |
| V. | CH3 – CH2 – O – CH2 – CH3 |
| VI. | CH3 – O – CH2 – CH2 – CH3 |
| VII. | \[\begin{array}{cc} \ce{CH3 - O - CH - CH3}\\ \phantom{...}|\\ \phantom{......}\ce{CH3} \end{array}\] |
Identify the pairs of compounds that represents chain isomerism.
Concept: undefined >> undefined
Compounds with same molecular formula but differing in their structures are said to be structural isomers. What type of structural isomerism is shown by
CH3 – S – CH2 – CH2 – CH3
And
\[\begin{array}{cc}
\phantom{.....................}\ce{CH3}\\
\phantom{................}/\\
\phantom{}\ce{CH3 - S - CH}\\
\phantom{...............}\backslash\\
\phantom{....................}\ce{CH3}
\end{array}\]
Concept: undefined >> undefined
Why does SO3 act as an electrophile?
Concept: undefined >> undefined
Match the terms mentioned in Column I with the terms in Column II.
| Column I | Column II |
| (i) Carbocation | (a) Cyclohexane and 1-hexene |
| (ii) Nucleophile of | (b) Conjugation of electrons of C – H σ bond with empty p-orbital present at adjacent positively charged carbon. |
| (iii) Hyperconjugation | (c) sp2 hybridised carbon with empty p-orbital |
| (iv) Isomers | (d) Ethyne |
| (v) sp hybridisation | (e) Species that can receive a pair of electrons |
| (vi) Electrophile | (f) Species that can supply a pair of electrons |
Concept: undefined >> undefined
Assertion (A): Pent- 1- ene and pent- 2- ene are position isomers.
Reason (R): Position isomers differ in the position of functional group or a substituent.
Concept: undefined >> undefined
The molecules having dipole moment are:
(i) 2,2-Dimethylpropane
(ii) trans-Pent-2-ene
(iii) cis-Hex-3-ene
(iv) 2, 2, 3, 3 - Tetramethylbutane.
Concept: undefined >> undefined
Assertion (A): The compound cyclooctane has the following structural formula: 
It is cyclic and has conjugated 8π-electron system but it is not an aromatic compound.
Reason (R): (4n + 2)π electrons rule does not hold good and ring is not planar.
Concept: undefined >> undefined
