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Thursday, August 5, 2021

Penetration Effect: Penetration Power:

The probability of an electron which allows an electron to get close to the nucleus is known as penetration effect. It is known as the proximity of the electron in the orbital to the nucleus.

(1)  The relative penetration power of sub shells within same shell (same value of n) follow the order as:

                                        s>p>d>f

We consider it for each shell and sub shell as the relative density of the electrons near the nucleus of atoms. It is clear that the ‘S’ electrons have greater probability of coming closer to the nucleus than the P, d or f electrons of the same principal energy shell. 

(2) For different values of shell (n) and sub shell (l), decreasing penetrating power of an electron follows as:

             1s>2s>2p>3s>3p>4s>3d>4p>5s>4d>5p>6s>4f....

(3) In other words, ‘S’ electrons penetrate (more nearer) more towards the nucleus than the ‘P’ electrons and the penetrating power of the electrons in the given principal energy shell varies as S> P> d>f. Thus the ‘S’ electrons experience more attraction from the nucleus than the p d or f electrons of the same principal energy shell.

Therefore, greater energy required to remove out electron from‘s’ orbital than ‘p’, d and ‘f’ orbital. Thus the ionization potential for pulling out an ‘s’ electron is maximum  and it decreases in pulling out a p , d or f electron of the same principal energy shell.

(4) Ionization potential or Ionization enthalpy of an atom is directly proportional to penetration power of orbitals.

Application of Penetration effect:

Example: Ionization energy of Boron is smaller than Beryllium even though effective nuclear charge is higher?

Solution: The electronic configurations of Boron and Beryllium are (5B=1S2,2S2,2p1) and (4Be =1S2,2S2).

In Boron the outermost electron is present in the 2p orbital (low penetration power) and is less strongly bound than the electron present in a 2S orbital of Beryllium(Have more penetration power), which will has a higher Zeff. It is easier to ionize the Boron atom.

Related Questions:

(1) What are the Amphoteric metals ? gives Examples.

(2) Name of total metalloids present in periodic table ?

(3) Total numbers of elements which are liquid at normal temperature is ?

(4) What is Mendeleev's periodic table ? give important features and draw back of Mendeleev's table.

(5) What is atomic density ? give the periodicity of atomic density in periods and groups.

(6) What is atomic volume ? and what is periodicity of atomic volume in groups and periods ?

(7) Why there are 2, 8 and 8 elements in first, second and third periodic of periods table respectively ? Explain.

(8) In alkali metal group which is the strongest reducing agent in aqueous solution and why?

(9) The electron affinity of sulphur is greater than oxygen. Why?

(10) The first ionization energy of carbon atom is greater than that of boron atom, whereas reverse is true for the second ionization energy. Explain.

(11) The electronegativities of B, Al, Ga are 2.0, 1.5, 1.6 respectively. The trend is not regular. Explain.

(12) Li2CO3 decomposes on heating but other alkali metal carbonates don’t. Explain.

(13) Of all noble metals, gold has got a relatively high electron affinity. Explain.

(14) What are the increasing order of ioni radii of first group elements in water ?

(15) What are the increasing order of molar conductivity of first group elements in water ?

 

Metallic radius or Crystal radius:

Metallic radius or Crystal radius:

(1) The term crystal radius is used to denote the size of atoms in metal.

(2) Metal atoms are closely packed spheres in metallic crystal. The metal atoms are supposed to touch one another in crystal.

(3) Metallic radius is defined as one half the distances between the centres of the nuclei of two atoms in a metallic crystal.

(4) Metallic radius is determined by X-ray diffraction method.

(5) Metallic radii are about 10 to 15 % higher than the single bond covalent raddi of those elements. Thus single bond covalent radius is smaller than the metallic radius due to the no overlapping of atomic orbital in metallic bond.

Vander Waal’s radius > Metallic radius > Covalent radius

(6) For the simplicity the term atomic radius is used for covalent radius as well as metallic radius depending on whether the element is a non-metal or metal. However, the atomic radii of inert gases are expressed in the terms of Vander Waal’s radii.

(7) Metallic radius is inversely proportional to the metallic bond strength.

(8) More metallic radius –loose crystal packing-less bond strength. (BCC)

(9) Less metallic radius –Tight crystal packing (FCC) - high bond strength.(HCP)

(10) For non-metal, atomic radius means covalent radius.

(11) For metal, atomic radius means metallic radius.

(12) For inert gases, atomic radius means Vander Waal’s radius.


Vander Waal’s radius or Collision radius:


Related Questions:

(1) What are the Amphoteric metals ? gives Examples.

Vander Waal’s radius or Collision radius:

 (1) The Vander Waal’s radius is defined as one half of the distance between the nuclei of two adjacent identical atoms  belongging to two neighbouring molecules of an elements in the solid state.


(2) The name Vander waal’s radius is used because of the force existing between yhe molecules are the vander waal’s forceof attractions. And Vander Waal’s forces are directly proportional to the molecular weight or atomic weight (in inert gases).

(3) These force of are maximum in solid state and absent in gaseous condition. In liquid state the magnitute is very small so Vander waal’s radius determine in solid state only.

(4) The Vander Waal’s radii is also known as non bonded radii.

(5) The Vander Waal’s radii is determined by X-rays difffraction studies.

(6) In molecules of non-metals both covalent and Vander Waal’s radius exists.

(7) The Vander Waal’s radii is always greater than covalent radius of a given elements. And also greater than that of all known radius.

(8) The Vander Waal’s radius is generally two times of Covalent radius

            Vander Waal’s and Covalent radii of some elements in Angstrom.

Elements

H

N

O

F

Cl

Br

Vander Waal’s radius

1.2

1.5

1.4

1.35

1.80

1.95

Covalent  radius

0.35

0.75

0.73

0.72

0.99

1.14

(9) The noble gases do not from covalent bonds. Thus in crystal of noble gases no chemical forces operated between the atoms. It is only the Vander Waal’s forces prevailing in these atoms. Thus for noble gases in the solid state the crystal radii (atomic radii) are actually Vander Waal’s radii.

(10)   Vander Waal’s radius > Metallic radius > covalent radius.

Metallic radius or Crystal radius:

Trends:

(1) In a Period:

While we move from left to right along period, atomic radius generally decreases.

(2) In a Group:

In a given  group as one moves from top to bottom atomic radius increases.

Related Questions:

(1) What are the Amphoteric metals ? gives Examples.

How many hydrogen bonded water molecules are present?

The maximum number of hydrogen bonds formed by a water molecule in ice is four (4).

Each water molecule can form two hydrogen bonds involving their hydrogen atoms and two further hydrogen bonds formed by the hydrogen atoms attached to adjacent water molecules. These four hydrogen bonds optimally arrange themselves tetrahedrally around each water molecule as found in ordinary ice.

Related Questions:

(2) What is the temperature at density of water is maximum ?

How many molecules form coordinate bonds in CuSO4.5H2O?

In Cupper Sulphate pentahydrate (CuSO4.5H2O) Cu is coordinated with 4 water molecules and two more oxygen atoms from Sulphate ion. And hence the coordination number of Cu (II) ion is six and hybridization is sp3d2 with distorted octahedral geometry. Now fifth water molecule is hydrogen bonded and is deeply embedded in crystal.

Thus it is clear that four (4) water molecules are coordinated and one (fifth one) water molecule is bonded with hydrogen bond. And its formula also written as [Cu(H2O )4SO4].H2O

Releted Questions:

(1) What is the structure of Blue vitriol (CuSO4) .5H2O also represent the H-Bond with water molecules?

(2) Why bond angle of hydrides of group 15, decreases down the group?

(3) Why SF6 behave inert towards hydrolysis?

(4) What are the SESQUI OXIDES ? give the examples.

(5) Arrange in increasing order of extent of hydrolysis [ CCI4, MgCI2, AICI3, PCl5, SiCI4].

(6) Why SF6 behave inert towards hydrolysis?

(7) Although Sulphur contain vacant d-orbital but SF6 does not under go hydrolysis. Why ?

(8) Phosphorus can form PCl5 but nitrogen can not form NCl5 why?

(9) Why PCl3 hydrolysed while NCl3 can not be hydrolysed?

(10) CCl4 can not be hydrolysed but SiCl4 can be. Why?

(11) Silianol (SiH3OH) is more acidic than methanol (CH3OH) why?

(12) How many hydrogen bonded water molecules does CuSO4.5H2O have?