Chemical Bonding Flashcards
Definite metallic bonding
Metallic bonding is the electrostatic attraction between positively charged cations and the sea of delocalised negatively charged electrons
Factors affecting strength of metallic bonding
- number of valence electrons contributed to sea of delocalised electrons (by higher charged cations)
- size of cation (smaller size of cation, stronger metallic bond)
Define ionic bonding
Ionic bond is the electrostatic forces of attraction between oppositely-charged ions
What factors affect coordination number?
Coordination number is the number of ions that surround another ion of opposite charge.
Factors:
1. Cationic and anionic radius. (larger cationic radius, more anions can surround, higher coordination number)
2. Cation to Anion ratio
Factors affecting strength of ionic bond
lattice energy= q+q-/r+ + r-
Factors determining covalent character in ionic bonds
- higher charge density of cation = charge/cationic radius.
- higher charge density, higher polarising power - larger electron cloud of anion (more electrons or larger anionic radius), the anion is more easily polarised
-AlCl3, AlBr3 and many Be compounds are covalent
Define covalent bonding
Covalent bonding is the electrostatic forces of attraction between a shared pair of electrons and positively-charged nucleus.
Draw bonding in Al3Cl6 and ammonium ion
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Criteria for dative bond
Donor atom has lone pair of electrons
Acceptor atom is electron deficient
State the shapes and bond angles for species
2EP:
2 bp –> Linear, 180
3EP:
3 bp –> trigonal planar, 120
2 bp, 1 lp –> bent, 110-120
4EP:
4 bp –> tetrahedral , 109.5
3 bp, 1 lp –> trigonal pyramidal, 107
2 bp, 2 lp –> bent, 105
5EP:
5 bp –> trigonal bipyramidal, 90&120
4 bp, 1 lp –> see-saw, 90&120
3 bp, 2 lp–> T-shaped, 90&120
6EP:
6 bp–> octahedral, 90
5 bp, 1 lp–> square pyramidal, 90
4 bp, 2 lp –> square planar, 90
State the VSEPR theory
-Electrons are negatively-charged and repel each other. Hence electron pairs around the central atom of a molecule are arranged as far apart as possible to minimise electrostatic repulsion and maximise stability
- Lone pair of electrons are closer to central atom and repel more than bonding electrons. Hence lplp repulsion > bplp repulsion > bpbp repulsion
Explain the effect of electronegativity on bond angle. Taking H2O and H2S as an example.
- Both H2O and H2S are covalent molecules with 2 bond pairs of and 2 lone pairs of electrons.
- In H2O, O has a greater electronegativity than S in H2S.
- Hence, the bond pair of electrons
are attracted closer to the central atom O, resulting in greater repulsion between thebond pairs of electrons of O in H2O. - Hence, H2O has a larger bond angle than H2S.
Explain the difference in C-C bond length
A sp3 hybrid orbital has more p character than a sp2 hybrid orbital and it is longer/more diffuse. Hence, a sp3 hybrid orbital undergoes less effective overlap, giving rise to longer
bond length and weaker bond.
Explain how idid attractions arise
- As electrons are constantly moving, there could be instantaneous dipole formed when there are more electrons formed on one side of the molecule. Hence there could be a small partial positive charge on one atom and small partial negative charge on the other atom.
- When a neighbouring molecule approaches, this instantaneous dipole induces a temporary dipole on the neighbouring molecule by attracting or repelling its electrons.
- This intermolecular forces of attraction between 2 molecules of opposite partial charged are called idid.
Explain factors affecting covalent bond strength. (covalent bond between atoms !)
- effectiveness of overlap of orbitals
(size of atomic orbital) smaller atoms can approach each other more closely, more effective overlap, stronger bond and shorter bond length - bond order
triple bond>double bond>single bond - bond polarity
greater EN diff, more polar bond, stronger the bond