Popular Chemistry Online: P-block elements -Comparative study of properties of different groups 15-18 of p-block

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Sunday, September 27, 2020

P-block elements -Comparative study of properties of different groups 15-18 of p-block

P-block elements-

 ·       Those elements in which last electron goes in p-orbital are known as p-block elements.

 ·       Consists of elements of group 13-18 of the periodic table 

·       Their valence shell electronic configuration is ns2np1-6 (except helium 1s2

Comparative study of properties of different groups 15-18 of p-block 

s. 

no 

properties 

Gr-15 

Gr-16 

Gr-17 

Gr-18 

A 

Atomic   properties 

 

 

 

 

1 

Elements 

N P As Sb Bi 

O S Se Te Po 

F Cl Br I At 

He Ne Ar Kr Xe Rn

2 

General valence shell Electronic configuration 

ns2np3 

ns2np4 

ns2np5 

ns2np6 

3 

Atomic size/ 

Ionic size- Increases down the group (because of increasing in No. Of shell or shelding effect ) while decreases in a period with increase in nuclear charge 

 

Increases down the group 

 There is considerable increase in covalent radii from N to P but from As to Bi only small increase observed 

Due to least shielding effect of completely filled d/f orbital 

Increases down the group  

Increases down the group 

 

Increases down the group 

 

4 

Ionization enthalpy 

Decreases down the group with increase size 

Decreases down the group with increase size 

 

Decreases down the group with increase size 

 

 

Decreases down the group with increase size 

 

 

5 

Electron gain enthalpy 

Decreases down the group with increase size 

 

Decreases down the group with increase size  

Exception - O has less (-)ve than S(because small size and high electron density in oxygen  

From S to Po again less negative 

 

Decreases down the group with increase size 

Exception-F has less (-)ve 

 electron gain enthalpy than Cl  

 

No. Tendency to get electron 

So, have positive EGE 

Physical properties 

 

 

 

 

Metallic character 

Increase on moving down 

N,P-Non-Metal 

As,Sb –Metalloid 

Bi- Typical metal 

Increase on moving down 

O,S- Non metal 

Se, Te-Metalloid 

Po-metal 

Increase on moving down 

F, Cl-gas 

Br- liquid 

I-solid 

Increase on moving down 

 

MP/BP 

MP first increases from N to As  

due to increase in atomic size and then decreases to Sb and Bi due to increase in tendency to form three covalent bonds instead of five covalent bonds with increase in size because of inert pair effect 

While BP regularly increases 

Increase down the group  

Exception 

Large difference in mp/bp of O and S since O is diatomic while S is polyatomic Po has lower bp/mp than Te 

Due to weak Vander Waals force because of max inert pair effect in Po.  

Increases 

increases 

density 

increases 

increases 

 

increases 

 

increases 

 

allotropy 

Except N and Bi , all show 

All show 

no 

No.  

C  

Chemical property 

 

 

 

 

Oxidation state 

Show –3 +3 +5 

-The stability of –3 O.S decrease down the group with increase metallic character 

-The stability of +5 O.S decrease down the group due to inert pair effect 

-The stability of +3 O.S increase down the group Due to inert pair effect 

-Nitrogen shows +1 to +4 Oxidation state 

So, it shows disproportionation rex (an element exists in reduced as well as oxidized 

3HNO2 ------> HNO2 +2NO + H20 

 

O show   -2  

   -1(H2O2)

   +2(OF2)  

Other +2,+4,+6 

The stability of +6 O.S decrease down the group due to inert pair effect 

-The stability of +4 O.S increase down the group Due to inert pair effect 

 

All exhibit 

    –1 o.s

Cl Br I show +1, +3, +5 ,   +7 

 Only Xe and Kr form compound only 

hydride 

EH3 

H2E 

HE 

no 

Stability α bond dissociation enthalpy 

Decreases down in the group 

With decrease in bond dissociation enthalpy 

Decreases down in the group 

Decreases down in the group 

 

----- 

Reducing nature α 1/E –H bond dissociation 

Increases down in group 

With decrease in bond dissociation enthalpy 

 

 

Except H2O all are reducing agent 

Increases down in group 

Increases down in group 

 

---- 

Basicity α availability of lone pair 

 Behave as Lewis base 

Basic nature Decreases down in the group 

(Electron density per unit volume) 

Decreases down in the group 

 

Decreases down in the group 

 

------- 

Acidic character  

α   1/E-H bond dissociation enthalpy 

Increases down in group 

 

 

 

 

 

1.Bond angle 

Decreases down in group 

NH3> AsH3> SbH3> BiH3 

With decrease in electronegativity 

2.bp decrease from N to P then increase up to Bi  

Bp of NH3 > Bp of PH3 since NH3 associated with hydrogen bond while interparticle force in PH3 is Vander Waals force. Its strength increases up to Bi with size, therefore bp increase again from as to Bi  

 

Increases down in group  

-due to increase in size of atoms, the distance between central atom and hydrogen increases on moving down ward in a group which favours the release of hydrogen as proton (it is the reason of week bond) 

-H2S is gas while H2O liquids due to presence of hydrogen bond in H2O i.e water molecules associated with hydrogen bond 

bond angle decreases down in group in various hydride of this group 

 

 

Increases down in group 

 

------- 

Oxides 

Form two type of oxides E2O3, E2O5 

Oxide of N and P-acidic 

As and Sb – amphoteric 

BiO3-basic predominantly 

EO2, EO3 

Forms but most of them unstable 

F forms OF2, O2F2 

Cl, Br,I form oxide containing range of oxidation state of halogen from +1 to +7 o.s 

--Mainly covalent bond due to small difference 

--->stability of oxide of halogen decreases in the order –I >Cl>Br   

Due to polarity in oxide of iodine, pi-bond in Cl and O but these both not present in oxide of bromine 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


 
Difference between Inert Pair Effect and Shielding Effect 

s.no 

Inert Pair Effect 

Shielding Effect 

 

the reluctance of s-electrons pairs of the valence shell to participate in chemical bonding 

nselectrons are not able to participate because of strong hold of nucleus due to high penetration effect of s electrons or poor shielding effect of inner orbitals  

(since completely filled orbitals as (n-1) d10 (n-2) f14 are more dispersed)  

 

In multi electronic atoms the outermost electrons are shielded or screened from the nucleus by the inner electron.  as a result of this, outermost electron does not feel the full nuclear charge, this effect is called screening effect 

2 

It helps to explain the stability of lower oxidation states for heavier elements of a group. 

The shielding effect explains why electrons from the valence shell can be removed easily and size of atom on moving in a group increases 

 

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