T1- p Block LP2 Flashcards

1
Q

What is trend for covalent radii in periodic table?

A

It decreases from left to right and from bottom to top.

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2
Q

What is Slater’s rule?

A

The outermost electrons feel a nuclear charge which is less than the actual nuclear charge, because of shielding effects from othermost electrons.

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3
Q

How to calculate effective nuclear charge?

A

Z*=Z-s, where Z is an actual nuclear charge, s-shielding constant.

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4
Q

What are the groupings when estimating shielding constant?

A

(1s) (2s,2p) (3s,3p) (3d) (4s,4p) (4d) (5s,5p) etc.

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5
Q

How much s contribute for each electron that has the same principle quantum number in the same (ns,np) (nd) d=group?

A

s=0.35

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6
Q

How much s contribute for each electron in the (n-1) shell?

A

s=0.85

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7
Q

How much s contribute for each electron in the (n-2) shell or lower?

A

s=1.00

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8
Q

What is the difference in estimating shielding constant when looking at an electron in an nd or nf orbital?

A

Each of the other electrons in the (nd,nf) group contributes 0.35, but the rest of electrons in lower groups contributes 1.00.

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9
Q

What is the trend of effective nuclear charge in periodic table?

A

It increases from left to right and from top to bottom.

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10
Q

What is the trend of ionisation in periodic table?

A

It decreases from left to right and from top to bottom.

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11
Q

What is covalent radii?

A

A covalemt radius is defined as half the length of a symmetrical homonuclear element bond.

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12
Q

What is cation?

A

A poistively charged ion.

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13
Q

What is anion?

A

A negatively charged ion.

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14
Q

What is general trend of covalent radii and why?

A

It increases going down a group as valence electrons are further from the nucleus, and it decreases from left to right as effective nuclear charge increases.

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15
Q

Why within a particular group, highest occupied orbital energies increase from top to bottom and the s-p separation decreases?

A

Becaues we have higher principal quantum shells so electrons further away from nucleus.

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16
Q

Why Ga and Ge does not follow s-p separation decrease trend?

A

It is because 4p row is immediately proceded by full 3d row which lowers the energy of the s orbital.

17
Q

Why s and p energies decrease from left to right?

A

It is because efective nuclear charge increases for both, but s has better penetration compared to p so s decreases more.

18
Q

Why 4s orbital for As, Se, Be, and Kr are lower than expected?

A

Because effective nuclear charge increases from 3rd row it has strong effects on 4s.

19
Q

Why wlwctrons in p orbitals are less stable and higher in energy than s?

A

This is because the s orbital penetrates closer to the nucleus and experiences a greater stabilising effect from its positive charge.

20
Q

What is inner pair effect?

A

The tendency of the electrons in the outermost atomic s orbital to remain unionised or unshared in compounds of the group 13-16 elements.

21
Q

Waht is the order of group 13 stability of +1 state?

A

Al < Ga < In < Tl

22
Q

That is the order of group 14 stability of +2 state?

A

Si < Ge < Sn < Pb

23
Q

Why inner pair effect occur?

A

It is because strength of covalent bonds decreases down a group due to poor orbital overlap and bond enthalpy does not offset the rehybridisation energy cost. For example, for Pb to rearange electrons to sp3 type of configuration would cost more energy that the amount of energy contained in, for example, Pb-C bond.

24
Q

What are relativistic effects?

A

The heavier the elements the faster the outer electrons go.

Objects moving near the speed of light gain mass.

25
Q

What is direct relativistic orbital contraction?

A

When electron reaches a high percentage of speed of light it gain mass. So some orbitals contract and its energy is lowered.

26
Q

Which orbitals experience direct relativistic orbital contraction?

A

s- they stabilised the most because they have best penetration and p- they stabilised less as they have poorer penetration.

27
Q

Which orbitals experience indirect relativistic expansion?

A

d and f as a result of poor penetration and the contraction of s and p leaves them more shielded and less affected by effective nuclear charge.