Covalent Bonding Flashcards

1
Q

What is a ‘pure’ sybstance?

A

Uniform composition

Cannot be separated into simpler substances by physical means

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2
Q

Define hetero/homogeneous mixtures

A

Hetero - components can be seen

Homogenous - uniform composition

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3
Q

Element anion suffix

A

-ide

Eg. H- = hydride
S2- = sulfide

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4
Q

What is an oxoanion?

A

Oxygen bonded (1 or more double bonds) to a central atom of a polyatomic ion

Eg. CO3^2-
End in -ate
Carbonate

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5
Q

Relative energy of bonded atoms vs non-bonding

A

Bonded have LOWER energy

Due to stronger attractive forces between -ve and +ve particles

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6
Q

Define covalent bond

A

Electron pairs between bonded atoms attracted to both NUCLEI (positive particles, NOT CATIONS) of bonded atoms

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7
Q

Is ionic bond formation exo or endo?

A

EXO

Driven by ions coming together (lattice formation)

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8
Q

Bond dipole moment units of measurement

A

Debye

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9
Q

Describe the morse curve

A

Energy vs distance between two atoms

Starts high, falls below x-axis, increases and tends to 0

At the minimum point, atoms approach each other and lose potential energy, electron pair bond formed

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10
Q

Why do C, O, N form multiple bonds but larger atoms do not?

A

Multiple bonds require overlap of particular e- clouds

Better overlap, stronger bond when atoms are SMALL

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11
Q

Lewis diagrams order of atoms general rule

A

The more electronegative atom is usually outer

Eg. N2O has N-N-O

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12
Q

Formal charge rules

A

Sum of formal charges = overall charge

  1. Assign an atom bonding + 1/2 nonbonding e-
  2. LESS than #valence e- = POSITIVE charge (more positive than isolated atom)
    MORE = NEG
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13
Q

Why use formal charges to assess plausability

A

Relative plausability of lewis structures.

Separating charge requires energy, hence LOWER formal charges is a better representation of the species

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14
Q

Define resonance form

A

Energetically equivalent (same # bonding and nonbonding e-) structures differ only in e- position

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15
Q

What is the hybrid structure?

A

Has -ve charge delocalised, equivalent bonds

like all resonance forms combined

Of LOWER energy (less reactive) dud to delocalisation

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16
Q

VSEPR define

A

e- pair domains about an atom occupies regions in space which are AS FAR APART as possible to minimise repulsion

17
Q

four electron areas possible shapes

A

all occupied = tetrahedral
3 occupied = trigonal pyramid
2 occupied = bent 109.5

18
Q

5 electron areas possible shapes and angles

A

all occupied = trigonal bipyramidal
4 occupied = see saw
3 occupied = t-shaped
90 and 120 degree angles

19
Q

6 electron areas possible shapes and angles

A

all occupied = octahedral
5 occupied = square pyramidal
4 = square planar

20
Q

regular bond angles apply ONLY IF…

A

all e- domains are equivalent.

non-bonding e- pair domains occupy MORE space.

21
Q

What property does bond strength affect?

A

the reactivity (energy required to break bond)

22
Q

trend in the strength of bond in relation to atom size

A

bonds between SMALLER atoms are SHORTER and STRONGER

23
Q

strength of multiple bonds in relation to single

A

multiple = SHORTER and STRONGER than single.

24
Q

define covalent bond in terms of orbitals

A

merging / overlap of orbitals and pairing of electron spins

25
Q

sigma bond

A

SINGLE BOND.

two e- in an orbital with cylindrical symmetry about the bond axis.
e- density concentrated between the nuclei of the bonding atoms. (bonding e- are localised)

eg. singly occupied pz orbital and s or another pz
(pz is taken as the orientation along bond axis)

26
Q

pi bond

A

DOUBLE bond

formed by overlap of orbitals in a side-by-side fashion, lobes either side of the internuclear axis.
e- density concentrated above and below the plane of the nuclei of bonding atoms.

eg. two singly occupied px or py orbitals

27
Q

triple bond (in terms of pi and sigma)

A

1 sigma, 2 pi bonds

28
Q

what is a hybrid orbital?

A

blended valence orbital, so they are energetically equivalent

linear combination (addition)

29
Q

number of hybrid orbitals =

A

number of atomic orbitals combined.

eg. 1s + 3p makes 4 identical sp3 hybrid orbitals

30
Q

hybrid and shape - how do decide what hybrid set to use

A
#hybrid orbitals required at a particular atom = 
#sigma bonds + # non-bonding e- pairs
31
Q

how do hybrid orbitals form sigma bonds?

A

can overlap with hybrid OR s-orbitals on adjacent atoms.

32
Q

overall e- density at an atom =

A

sum of e- densities of the occupied orbitals.

atom w/ hybridised orbitals has the same overall e- density as unhybridised orbitals.

33
Q

what are temporary dipoles

A

Van der Waals forces
e- cloud in adjacent uncharged particles induces temporary dipoles when particles are close (liquid)

present in condensed phase of EVERY molecule

larger e- cloud = polarised to greater extent = stronger attractive forces (hence Tb increases as size increases)

34
Q

permanent dipoles

A

exist in a polar molecule with partial charge, when there is an electronegative element (O, N, halogen) present.

35
Q

hydrogen bonding

A

when H bonded to O, N or F, a very strong dipole is formed, making H very strongly (partially) positive.

stronger than temporary/permanent dipoles, apt 1/10 the strength of a covalent bond