P-Block Flashcards

(49 cards)

1
Q

What is ionisation energy?

A

an always positive energy required to remove an electron from atom in its ground state

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2
Q

Name generic trends in ionisation energy

A

increases from left to right along periods and decreases down groups

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3
Q

What does the value of IE depend on

A

distance between nucleus and the electron

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4
Q

Why is there often deviations with trends of IE

A

if new shells are used or symmetry can be restored

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5
Q

Why do Ga and Ti have higher IE?

A

as D-Orbitals are occupied so more shielding is present

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6
Q

What is electron affinity?

A

Energy released when an atom/ion gains an electron

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7
Q

What are the general trends with electron affinity

A

increases from left to right along periods due to higher nuclear charge and decreases down groups due to shells being further away from nucleus

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8
Q

What is Slaters rule

A

outermost electrons feel a less nuclear charge than the actual nuclear charge due to shielding effects from inner electrons

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9
Q

What happens t the radius of atoms from left to right and why

A

radius contracts due to the increase of nuclear charge

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10
Q

What happens to the radius of atoms down groups

A

radius increases as number of shells increases

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11
Q

Why are P-electrons higher in energy?

A

they penetrate the nuceus less than the s orbitals so p-orbitals are less stabilised

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12
Q

What is the inert pair effect

A

tendency of electrons in outermost atomic s-orbital to remain unshared in compounds

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13
Q

What happens to bond strengths down a group?

A

Bonds become weaker and longer as the valence orbitals are larger and so less electron dense so less overlap

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14
Q

Why do only first row elements form multiple bonds

A

the 2p pi orbitals are small and electron dense so give good overlap

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15
Q

Why is the B-F bond so strong

A

small, electron dense orbitals so very effective overlap forming a polar covalent bond

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16
Q

What is the general trend for bond energy of hydrides

A

bond energies increase from left to right due to no lone pairs on H and greatest electronegativity on RHS

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17
Q

What is a triel bond

A

bond between a group 13 element and a halide, which act as Lewis acids

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18
Q

What shape is the molecule BF3

A

trigonal planar due to its sp2 hybridisation

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19
Q

Why is BF3 a stronger Lewis acid than BI3

A

because iodine has larger more diffuse orbitals so less efficient overlap

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20
Q

give 2 examples of hydride reducing agents

A

LiAlH4 and NaBH4

21
Q

What are Wades rules used for?

A

used to explain structures of boron hydrides and work out number of pairs of electrons for bonding

22
Q

roughly explain wades rules

A

each BH unit donates 2 electrons, any extra hydrogens also donate one electron each, negative charge means an extra electron, number of pairs -1 means number of vertices in structure

23
Q

what is a carborane?

A

where 1 or more B atoms is replaced with a Carbon atom. wades rules can also be used for carboranes

24
Q

what are allotropes

A

different structural forms of the same element

25
what are the general trends in oxidation state down group 14
+4 OS is most common at the top of the group but as you go down the gorup +2 is more stable due to the inert pair effect
26
what happens to the stability of the hydrides as you go down the group 14
stability decreases down group 14 due to increasing bond lengths
27
whats the difference between carbon halides and other group 14 halides
CX4 is hydrolytically stable but all the others are volatile and susceptible for nucleophilic attack as X is a good leaving group, bond strengths increase down the group as an increasing electronegativity difference
28
how can halides form silanes
halide + alcohol = silane
29
how are silicones formed?
hydrolysis of silylhalides to form silanol, then condensation of silanol to form siloxane. different monomer units are needed for terminal, chain and cross linking units.
30
why is the Si-O bond so strong?
P-pi D-pi bonding. the filled 2p orbital of O donates into empty 3d orbital of Si. the bond is so strong it only reacts with fluorinating agents
31
give an example of an organosilane and its properties
TMS, which is the reference for NMR, stable due to shielding and not polar bonds.
32
why cant low period elements easily make triple and double bonds, how can you make them form pi bonds?
sigma bonds are preferred to pi bonds, but by using bulky sterically hindering groups can block oligomerisation to stop metal centres form polymerising via sigma bonds
33
Why are lower valence compounds favoured by lead
the inert pair effect meaning and the relativistic effect
34
explain the general trends in ionisation energy group 15
Ionisation energy decreases due to the increase in distance from electron to nucleus
35
what range of oxidation states does group 15 have?
varies from -3 to +5
36
why is the P=O bond so strong
P-pi D-pi bonding by donation of p electrons of O into Dorbital of P, often a driving force for mamy reactions. explains why some phosphorus is very reactive with oxygen
37
What is P-pi D-pi bonding
when electron density from a p-orbital donated into another atoms d-orbital to form very strong covalent bonds
38
What oxidation states is phosphorus in phosphorus oxides
Phosphorus 5 or phosphorus 3
39
Describe the nitrite ion
NO2- ion, the nitrogen is 3+ oxidation state, trig planar shape
40
Describe the nitronium ion
NO2+ ion, Nitrogen in 5+ oxidation state, linear shape
41
what is the general trend with hydride bonding down group 15
bond energy decreases down group, so does the bond angle, due to valence electrons being further away from nucleus
42
why does NH3 have a relatively high BP for group 13 hydrides
has high polarity and strong H bonding, is basic
43
what makes phosphorus a good ligand
can be used as PR3 which takes a cone angle shape which accepts electrons from metal orbitals
44
What are the two halide formations for group 15 elements
MX3 or MX5 but only MX5 can be formed with smaller halides due to strong bonds needed
45
Describe properties of PF3
gas at room temp, similar ligand to CO as the electronegativity of F lowers energy of the P 3d orbitals giving good pi backbonding
46
how do you find pKa
pKa = -log Ka
47
what does a small pKa mean
small pKa = large Ka = strong acid
48
What are Dragos rules used for? what are they?
if Dragos rules are true, no need to consider hybridisation for the central atom (pure p-orbital bonding) -if central atom has at least 1 lone pair -if central atom belongs to group 13,14,15,16 between 3-7 period -if electronegativity of surrounding elements in 2.5 or less -if sum of sigma bonds + lone pairs =4
49
What are wades rules used for? what are they?
predicting the structure of boranes/carboranes cluster bonding each BH/CH unit donates 2 electrons, each bridging H atom donates 1 e, negative charge adds 1 e, if we have n pairs then polyhedron formed has n-1 vertices. compare number of vertices to number of non H atoms and see if your short. closo, nido or arachno