Chem Bonding Flashcards

1
Q

covalent bond

A

Electrostatic forces of attraction between the shared electron and the positively charge nuclei due to the sharing of electrons through overlapping of orbitals

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2
Q

dative covalent bond

A

an atom donates a lone pair of electrons into an empty orbital of another atom for sharing

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3
Q

factors affecting strength of covalent bond

A
  1. bond order
    as bond order increases, the number of bonding electrons within the inter-nuclei region increases. the electrostatic forces of attraction for these electrons increases
  2. effectiveness overlap of orbitals
    the larger the atom, the larger and more diffused the orbitals, the less effective the overlap of orbitals and the weaker the covalent bond
  3. polarity of covalent bond
    the greater the difference in electronegativities of the bonding atoms, the more polar the bond, the stronger the attractive forces between the S+ and S- that strengthens the covalent bond
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4
Q

ionic bond

A

strong electrostatic forces of attraction between oppositely charged ions in giant ionic lattice structure

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5
Q

Factors affecting strength of bonds

A
  1. Charge of ions
  2. Ionic radius

Greater charge of ions, smaller ionic radius, the stronger the ionic bond.
difference in charge is more important than difference in ionic radius

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6
Q

metallic bonds

A

strong electrostatic forces of attraction between the metal cations and sea of delocalised electrons in giant metallic lattice structure

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7
Q

factor affecting strength of metallic bond

A
  1. charge density of the metal cation
    greater the charge and the smaller the size of the ion, the stronger the metallic bond
  2. the number of valence electrons
    the large number of valence electrons implies that the large number of sea of delocalised electrons
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8
Q

Instantaneous dipole- induced dipole

A

esfoa between temporary diploles. exist in all simple covalent molecules and noble gases

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9
Q

strength of id-id

A
  1. no of electrons
    the larger the no of electron, the more polarisable is the electron cloud, resulting in stronger idid
  2. surface area of molecules (isomers)
    straight chain molecule has a larger surface of interaction for more extensive id-id than a branched isomer
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10
Q

permanent dipole-permanent dipole

A

esfoa between polar dipoles which exist between polar molecules

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11
Q

strength of pdpd

A

magnitude of net dipole moment
- difference in electronegativity
- arrangement of polar covalent bonds

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12
Q

hydrogen bonds

A

esfoa between electron-deficient H atom that is bonded to O, F or N atom and lone pair of electrons on a highly electronegative O, F or N atom

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13
Q

Strength of H-bonds

A
  1. Polarity of H-X bond
    the more polar the H-X bind, the stronger the H-bond
  2. extensiveness of inter-molecular H bonds
    - number of H atoms bonded to N/O/F atom
    - number of lone pairs on N/O/F atom
    - presence of intramolecular H-bond
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14
Q

if solute is soluble in solvent

A

energy that is released from the solute-solvent interaction is sufficient to compensate for energy needed to overcome the solute-solvent and solvent-solute interactions.

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15
Q

why are ALCL3, ALBr3 and Be CL2 covalent compounds

A

they are simple molecule structure due to high charge density of cation and high polarisability of anion.

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16
Q

Solubility of ionic compounds

A

generally soluble due to formation of favourable ion-dipole interactions between ion and water molecules.

some are insoluble due to highly exothermic lattice energy

17
Q

solubility of covalent simple molecules

A

generally insoluble in water as weak IMF interactions formed with water are weaker than H-bonds between water molecule