Explore topic-wise InterviewSolutions in Current Affairs.

This section includes 7 InterviewSolutions, each offering curated multiple-choice questions to sharpen your Current Affairs knowledge and support exam preparation. Choose a topic below to get started.

1.

Draw the structure of white phosphorus and red phosphorus. Which one of these two types of phosphorus, is more reactive and why ? Or Which allotrope of phosphorus is more reactive and why? Or Why is red phosphorus less reactive than white phosphorus. Or Draw the structural difference between white and red phosphorus.

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Solution :Both white and red phosphorus consist of `P_(4)` tetrahedra. In white phosphorus, the various `P_(4)` molecules are HELD TOGETHER by weak van der Waals forces of attraction. In each `P_(4)` molecule, the PPP ANGLE is only `60^(@)` (Fig. 11.31, page 11/127) which is much smaller than the NORMAL tetrahedral angle of `109^(@)-28`. As a result, there is considerable angle strain. Due to weaker forces of attraction and considerable angle strain, white phsphorus is very reactive.
In contrast, in red phosphorus, these `P_(4)` tetrahedra are joined together throughi covalent BONDS to give polymeric structure (Fig. 11.32, page 11/129).
Since it is difficult to break strong covalent bond as compared to weak van der Waals forces of attraction, therefore, white phosphorus is more reactive than red phosphorus.
2.

Draw the structure of the isotopes of hydrogen and distinguish them.

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SOLUTION :
3.

Draw the structure of PCl_(5). Or Solid PCl_(5) is ionic in nature.

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Solution :In the solid, `PCl_(5)` EXISTS as `[PCl_(4)]^(+)[PCl_(6)]^(-)` in which `[PCl_(4)]^(+)` SPECIES is tetrahedral while `[PCl_(6)]^(-)` species is octahedral as SHOWN :
4.

Draw the structure of P and Q.

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ANSWER :`(##RES_CHM_GOC_II_E01_007_A01##)`
5.

Draw the structure of (i) Mesitylene (ii) 1, 2, 3-trimethyl benzene

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SOLUTION :(i)
6.

Draw the structure of (i) BeCl_(2) (vapour) (ii) BeCl_(2) (solid).

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Solution :(i) In the vapour state, BECL, exists as a monomer with a LINEAR STRUCTURE.

(II)`BeCl_(2)` exists as a POLYMER in condensed (solid) phase.
7.

Draw the structure of (i) Acetic acid (ii) Water.

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SOLUTION :
8.

Draw the structure of (i) 1-ethyl-2-methyl cyclopentane (ii) 1-ethyl-2, 3-dimethyl cyclohexane (iii) 5-ethyl-2-methylcyclohex-1-ene

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SOLUTION :(i)
9.

Draw the structure of (i) 2-cyclopentyl propanal (ii) 2-cyclo-but-enyl propanal

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SOLUTION :(i)
10.

Draw the structure of H_(2) SO_(4) . What is hybridisation of S-atom in it ?

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Solution :`H-O-UNDERSET(O) underset(DARR)OVERSET(O) overset(UARR)S-O-H` . Hybridisation of S-atom is `sp^(3)`.
11.

Draw the structure of compound having C_(7)H_(8) and give number of sigma and pi bonds.

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Solution :It POSSESS three double `(PI). HC=CH`
it has `7C-C sigma` bond and 8C-H `sigma`-bond,
TOTAL 15 C-H `sigma` BONDS.



12.

Draw the structure of d-orbital (OrbitaI whose Azimuthal quantum no= 2).

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SOLUTION :d- ORBITAL has 5 ORIENTATIONS.
13.

Draw the structure of chromium pentoxide and predict the oxidation number of chromium in it

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Solution :The structure of chromium PENTOXIDE is given on the RHS
LET X be the O.N fo Cr then
X+(4-1)+ 1(-2) =0
or x=+6+
14.

Draw the structureof boricacid showinghydrogenbonding. Which speciesis present in water ? What is the hybridisation of boron in this species ?

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Solution :In water, boric acid is present in form of `[B(OH)_(4)]^(-)` SPECIES .
`B(OH)_(3) + 2H_(2)O RARR [B(OH)_(4)]^(-) +H_(3)O^(+)`
Since in thisspecies , `[B(OH)_(4)]^(-)`, Bis attachedto fourOH group , therefore , B is `SP^(3)` hybridized.
15.

Draw the structure of boric acid showing hydrogen bonding. Which species is present in water ? What is the hybridizations of boron in this species ?

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Solution :It has a layer structure in which planar `H_3BO_3` units are JOINED by HYDROGEN bonds forming hexagonal rings. Boric ACID is a weak monobasic acid. It is not a protonic acid but acts as a LEWIS acid by accepting electrons from a hydroxyl ion. In water, boric acid is present in the form of `[B(OH)_4]^(-)`species. The HYBRIDIZATIONS of boron in this species is `sp^3`.
`B(OH)_3+ 2HOH to [B(OH)_4]^(-) + H_3O^+`
16.

Draw the structure of BeCl_(2) in different physical states.

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SOLUTION :
17.

Draw the structure of BCl_(3).NH_(3) and AlCl_(3) (dimer).

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Solution :In `BCl_(2)` the CENTRAL B atom has six electrons in the valence shell. It is,therefore, an ELECTRON deficient molecule and needs twomore electrons to completeits octet. In otherwords, `BCl_(3)`actsas a Lewis acids. `NH_(3)`,on theother hand, has a lone pair of electronswhich it can donate EASILY. Therefore,`NH_(3)` acts as a Lewisbase. The Lewis acid `(BCl_(3))`and theLewisbase `(NH_(3))`combinetogetherto form an adduct as SHOWN below :

In `AlCl_(3)`, Al has sixelectronsin the velence shell. Therefore, it is an electrondeficient moleculeand needs two more electrons tocompleteits octet. In otherwords, `AlCl_(3)` acts as a Lewis acid.
Chlorine, on the other hand,has THREE lone pairs of electrons.
Therefore, to completeits octet, the central Al atom of one moleculeaccepts a lone pair of electronsfrom Cl atom of theother moleculeforming adimericstructureas shownabove.
18.

Draw the structure of AB_(4)L_(2) and AB_(7) type of molecules with example.

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SOLUTION :
19.

Draw the structure of AB_(2), AB_(3), AB_(3)L type of molecules with example.

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Solution :(i) `AB_(2)` : Number ot bond PAIRS = 2
Shape = Linear
Example : `BeCl_(2)`
(ii) `AB_(3)` : Number of bond pairs = 3
Shape = Tirgonal planar
Example : `BF_(3)`
(III) `AB_(2)L` : Number of bond pairs = 2
Number of lons pairs = 1
Shape = Bent (or) inverted V shape
Example : `NH_(3)`
` (##FM_CHE_XI_V02_C10_E03_170_S01.png" width="80%">
20.

Draw the structure of 4-hydroxy-3(2-hydroxy ethyl) hexanoic acid.

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Solution :`UNDERSET("4-hydroxy-3-(2 hydroxyethyl-hexanoic ACID)")(overset(6)CH_(3)-overset(5)CH_(2)-underset(OH)underset(|)(overset(4)CH)-overset(overset(CH_(2)OH)overset(|)(CH_(2)))overset(|)(overset(3)CH)-overset(2)CH_(2)-overset(1)COOH`
21.

Draw the structure (i) 1-(cyclo butyl)-2 (cylopropyl) ethane (ii) 2-carbomyl cyclobutane-1-carboxylic acid

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SOLUTION :(i)
22.

Draw the structure and write down the IUPAC name for the isomerism exhibited by the molecular formulae. (i) C_(5)H_(12)-Pentane (3isomers) (ii) C_(6)H_(14)-Hexane(5isomers)

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Solution :`(i) C_(5)H_(10)`
`(a) CH_(3)-CH_(2)-CH_(2)-CH_(2)-CH_(3) to n` PENTANE
`(b) CH_(3)-CH_(2)-underset(2-"methyl"-1-"but"-1"are")underset(CH_(3))underset(|)(CH)-CH_(2)`
`(c ) CH_(3)-overset(CH_(3))overset(|)underset(CH_(3))underset(|)(C )-CH_(3)to2`, `2`-Dimethyl propane
`(ii) C_(6)H_(14)`
`(a) underset(n-"hexane")(CH_(3)-CH_(2))-CH_(2)-CH_(2)-CH_(2)-CH_(3)to`
`(b) underset("pentane")(CH_(3)-underset(CH_(3))underset(|)(C )H)-CH_(2)-CH_(2)-CH_(3)to"Methyl"`
`(c ) underset(3"Methyl pentane")(CH_(3)-CH_(2)-CH)-CH-CH-CH_(2)-CH_(3)to`
`(d) CH_(3)-overset(CH_(3))overset(|)underset(CH_(3))underset(|)(C )-CH_(2)-CH_(3)to2"methyl pentane"`
`(e) CH_(3)-underset(CH_(3))underset(|)(C )H-underset(CH_(3))underset(|)(C )H-CH_(3)to2,2- "dimethyl"`
butone [These two compounds exhibits constitutional isomerism]
23.

Draw the structure and writedownthe IUPc name for the isomerism exhibited by the molecular formulae (i) C_(5)H_(10) -Pentene (3 isomers) (ii) C_(6)H_(12)-Hexene (5 isomers )

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Solution :`(i) C_(5) H_(10)-`Pentene(3 isomers )
(a) `CH_(3) - CH_(2) - CH_(2) - CH = CH_(2) to 1-` pentene(or)pent- ene
(b)`CH_(3)- CH_(2) - CH =CH - CH_(3) to 2-`PENTANE(or)pent -2-ene
(c ) `CH_(3) - UNDERSET( CH_(3)) underset(|) (CH ) - CH = CH_(2) to 3-`methyl- but -2- ene
(ii)`C_(6) H_(12)-`Hexzne(5 isomer )
(a) `CH_(3)- CH_(2)- CH_(2) - CH_(3)n = CH_(2) to ` Hex-1- ene
(b) ` CH_(3) - CH_(2) - CH_(2)- CH = CH - CH_(3) to`Hex -2-ene
(c )`CH_(3)- CH_(2)- CH - CH = CH_(2)- CH_(3) to`Hex -3-3ene
(d ) ` CH_(3)- underset( CH_(3))underset(|)(CH )- CH_(2) l - CH= C H_(2)to 4-`methyl-pene-1-ene
` (e )CH_(3) - underset(CH_(3) )underset(|)overset( CH_(3) ) overset( |) (C ) - CH = CH_(2) to3,3- `dimethylbut1- ene
Thesetwocompoundsexihibitsconstitutionisomerism
24.

Draw the structural formula of the following compounds. (i) N-ethyl-N-methylpropan-1-amine (ii) N,N-dimethyl benzenamine

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Solution :(i) `CH_(3)-CH_(2)-CH_(2)-OVERSET(CH_(3))overset(|)N-CH_(2)-CH_(3)` (II)
25.

Draw the structural formula of: (i) 4-methylpent-3-en-2-one (ii) pent-1-yne-3-one

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SOLUTION :(i) `CH_(3)-UNDERSET(CH_(3))underset(|)C=CH-underset(O)underset(||)C-CH_(3)` (ii) `CH_(3)-CH_(2)-underset(O)underset(||)C-C=CH`
26.

Draw the structural formula for 4,5 diethyl -3,4,5 trimethyloctane

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Solution :`CH_(3) -CH_(3) underset(H) underset(|) (C ) - underset(C_(2)H_(7) )underset(|) OVERSET( 4)(C ) - underset(C_(2)H_(5))underset(|) (C ) -CH_(7) -CH_(3)`
`(4,5` -DIETHYL -3.4trimethyloctane )
27.

Draw the staggered conformation of ehtane.

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ANSWER : `(##SPH_BSR_CHE_QB_XI_QP_E01_010_A01##)`
28.

Draw the sp^(3) hybridized C.

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Solution :In `SP^(3)` hybridization from `1s^(2)2s^(1)2p_(x)^(1)2_(y)^(1)2p_(2)` the orbitals `2s^(1)2p_(x)^(1)2_(y)^(1)2p_(2)` hybridization to give `sp^(3)` HYBRIDIZED C as FOLLOWS.
29.

Draw the sp^(2) hybridized C.

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SOLUTION :In `SP^(3)` HYBRIDIZATION, the `2s^(1),2p_(x)^(1),2_(y)^(1)` orbtials hybridization where as `2p_(2)` is not involves in hybridization.
30.

Draw the shapes of the following hybridorbitals:sp sp^(2) and sp^(3) .

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Solution :
All the HYBRID ORBITALS have same SHAPE . However , their sizes are in the order ` SP lt sp^(2) lt sp^(3)`
.
31.

Draw the sp^ hybridized C.

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SOLUTION :In SP hybridized C, the `2S^(1)&2p_(x)^(1)` is hybridizes where are `2p_(y)^(1)and2p_(x)^(1)` is not.
32.

Draw the shapes of 1s,2s and 3s orbitals.

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SOLUTION :
33.

Draw the shape of (i) XeF_(2) (ii) IOF_(5) (iii) XeOF_(4)

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SOLUTION :
34.

Draw the resonating structure of Phenoxide ion .

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SOLUTION :`C_(6)H_(5)O^(-)`
35.

Draw the resonance structurs for the following compounds?(a)CH_(3)CH = CHCHO (b) CH_(3)CH = CHC^(oplus)H_(2) (c) CO_(2)

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SOLUTION :
36.

Draw the resonating structure ofC_(6) H_(5) NH_(2) .

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SOLUTION :
37.

Draw the resonating structure of Nitrate ion.

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SOLUTION :NITRATE ION :
38.

Draw the resonating structure of (A) Ozone molecule (B) Nitrate ion

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SOLUTION :The resonating STRUCTURE of ozone MOLECULE may be written as

(B) The resonating structure of nitrate ion`(NO_(3)^(-))` is
39.

Draw the resonance structures of the following compounds : (i) CH_(2) = CH-underset(..)overset(..)(Cl):(ii) CH_(2) = CH - CH = CH_(2) (iii) CH_(2) = CH - underset(H)underset(|)(C) = O

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SOLUTION :
40.

Draw the resonance structures of the following compounds. (a) CH_(2)= CH= underset(..)overset(..)(C )l: (b) CH_(2)=CH-CH= CH_(2) (c ) CH_(2)= CH- underset(underset(H)(|))(C )=O

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Solution :(a) `CH_(2)= CH- underset(..)overset(..)(C )l: HARR overset(+)(C )H_(2) - CH= underset(..)(C )overset(+)(l):`
In ethenal, Cl is negative atom which give the non-bonding electron pair to the adjacent C-Cl and form `pi`-BOND.

In structure (A) 1-2 CARBON and 3-4 carbon, `pi`-electron pair respectively more in `C_(2)-C_(3) and C_(4)` so structure (B) form.
The `pi` electron pair of `C_(3)-C_(4)` shift on `C_(2)-C_(3) and C_(1)-C_(2) pi`-electron pair shift on `C_(1)`. So negative charge on `C_(1)` and positive charge on `C_(4)` possessive structure (C ) form
41.

Draw the resonance structures for the following compounds. Show the electron shift using curved-arrow notation. (a) C_(6)H_(5)OH(b) C_(6)H_(5)NO_(2) (c) CH_(3)CH = CHCHO (d) C_(6)H_(5) - CHO (e) C_(6)H_(5)-overset(+)(C)H_(2) (f) CH_(3)CH = CHoverset(+)(C)H_(2)

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SOLUTION :
42.

Draw the resonance structures for the following compounds. Show the electron shift using curved-arrow notation. (a) C_(6)H_(5)OH (b) C_(6)H_(5)NO_(2) (c ) CH_(3)CH= CHCHO (d) C_(6)H_(5)-CHO (e ) C_(6)H_(5)- overset(+)(C )H_(2) (f ) CH_(3)CH= CH overset(+)(C )H_(2)

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SOLUTION :(a) RESONANCE structures of `C_(6)H_(5)OH`:

(b) Resonance structures of NITROBENZENE:
(c ) Resonance structures of `CH_(3)CH= CHCHO`

(d) Resonance structures of `C_(6)H_(5)-CHO` (Benzaldehyde)

(e ) Resonance structures of `C_(6)H_(5)overset(+)(C )H_(2)` (Benzyl Carbocation):

(f) Resonance STRUCTURE of carbocations of
`CH_(3)-CH = CH-overset(+)(C )H_(2)` (But-2-en-1-yl)

Positive charge is displace by these structure
43.

Draw the resonance structures for the following compounds. Show the electron shift using curved-arrow notation. (a) C_6H_5OH (b) C_6H_5NO_2 ( c) C_6H_5 overset (oplus) CH_2 (d) CH_3CH=CHCHO ( e) CH_3CH=CH-overset (oplus) CH_2 (f) C_6H_5CHO (g) CH_2=CHOCH_3.

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SOLUTION :
.
`({:("Electropositive ELEMENT with POSITIVE cahrge"),("ELECTRONEGATIVE element with negative charge"):})`
44.

Draw the resonance structure of CO_2

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SOLUTION :`:UNDERSET(..)ddotO OVERSET(ɵ)-C-=O:^(+) HARR:ddotO=C=ddotO: harr:^(+)O-=C-ddotO:^(ɵ)`
45.

Draw the functional isomers for the formula C_(3)H_(6)O_(2) with their names.

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Solution :`C_(3)H_(6)O_(2)` : (i) `CH_(3)-CH_(2)-COOH` (Propanic acid)
(II) `CH_(3)-COOCH_(3)` (METHYL acetate)
46.

Draw the possible resonance structures for CH_(3) - underset(..)overset(..)(O)-overset(+)(C )H_(2) and predict which of the structures is more stable. Give reason for your answer.

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SOLUTION :The GIVEN carbocation has two resonance STRUCTURE i.e., (i) and (ii) are as under:
47.

Draw the polygon formulae for all the possible structural isomers having the molecular formula C_(5)H_(10).

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Solution :By polygon formulae, we mean CYCLIC formulae. `C_(5)H_(10)` has the FOLLOWING six polygon formulae :
48.

Draw the plot log V vs log T.

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<P>

SOLUTION :
PLOT of log P VS log V
49.

Draw the plot log P vs log V for Boyle's law.

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SOLUTION :This implies that at this value of pressure ATTRACTIVE and repulsive forces balance each other this pressure attraction DOMINATES and `Zlt1` above this pressure REPULSION DOMINATE and `Zgt1`.
50.

Draw the most stable conformer of N-methylpiperidine.

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ANSWER :`(##BSL_CHM_ISO_E01_149_A01##)`