3. Bonding Flashcards

1
Q

Exceptions to octet rule

A

H, He, Li, Be, B

Within or after period 3

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2
Q

Does a molec with polar bond always polar?

A

Nope, depends on cancelled out dipole moments

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3
Q

London dispersion forces

A

When a covalent bond contains slight unequal sharing of e- leading to constant polarization and counter polarization; type of van der Waals force; weakest of intermolecular forces
LDF = only intermolecular force in noble gases, but LDF = present in ALL molec. LDF inc with bigger atoms b/c they have more e- to interact —> more polarizable

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4
Q

Ionic bonding vs covalent bonding vs coordinate covalent bonding vs heterolytic rxns

A

When 1+ e- of atom with low IE = transferred to atom with high EA; from crystal lattice - large, organized arrays of ions vs when e- pair = shared b/w atoms with similar electronegativity; if pair = shared unequally —> polar vs when shared e- = contributed by only one of two atoms (ex: when Lewis base gives e- pair to Lewis acid) vs opposite of coordinate covalent bonding: bond breaks and both e- go back to one of the products

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5
Q

Bond energy vs bond dissociation energy/bond enthalpy

A

AVG ENERGY required to break all bonds into isolated, gaseous states; the more e- shared —> the more energy needed to break it
The higher the bond energy —> the shorter the bond length (ex: triple bonds vs double bonds) vs THE ENERGY IT TAKES TO BREAK A SPECIFIC BOND IN A GAS PHASE; always pos b/c it requires energy

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6
Q

Know which bond is strongest b/w triple, double, single, sigma and pi bonds. Why is single bond stronger than sigma bonds?

A

I pretty much laid it out for you. S orbitals have more overlap than p orbitals

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7
Q

How to find formal charge? How to find valence e-?

A
# ve- in free atom minus # of ve- in bonded atom
Group # on periodic table
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8
Q

Linear vs trigonal planar vs tetrahedral vs square planar vs trigonal bipyramidal vs octahedral angles and hybridization

A

180; sp vs 120; sp2 vs 109.5; sp3 vs 90; sp3d2 90,120,180; sp3d vs 90, 180; sp3d2, 6 sigma bonds and no lone pairs

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8
Q

Valence shell electron pair repulsion theory (VSEPR)

A

3D arrangement of atoms around a central atom is determined by repulsions b/w bonding and nonbonding e- pairs in valence shell of central atom

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9
Q

Electronic vs molecular geometry

A

Position of all bonding and lone e- pairs around central atom vs position of only bonding e- pair; uses coordination number - # of atoms that surround and bonded to central atom

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10
Q

Molecular orbital vs bonding orbital vs antibonding orbital

A

When 2 atoms form a cmpd —> atomic orbitals interact => molecular orbital vs signs of 2 atomic orbitals that are same vs 2 atomic orbitals that are different

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11
Q

Sigma bond vs pi bond

A

single bonds; head to head overlap, allows free rotation around axis vs double and triple bonds; parallel e- clouds overlap, doesn’t allow free rotation around axis

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12
Q

Which elements do H bonds?

A

F, O, N; H bonds = strongest type of dipole dipole interaction

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13
Q

How to determine higher bpts based on intermolecular forces?

A

Consider all the forces involved (dispersion forces, dipole-dipole, H bonds): Ionic bond = strongest, dispersion forces = weakest; if molec have 1+ type of forces —> higher bpt

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14
Q

How to determine largest dipole moment?

A

If linear and no dipoles cancel out —> strongest dipole moment. If bent or some dipoles cancel out —> weaker dipole moment

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15
Q

What is a conjugated system?

A

Alternating single bonds and multiple bonds; this allows pi e- to delocalized throughout unhybridized p orbitals or heteroatoms with lone pairs of e-

16
Q

S orbital vs p orbital vs node

A

Round and spherical, centered around nucleus vs 2 lobes located symmetrically around nucleus (like a dumbbell) vs area where probability of finding e- = zero (ie. At the nucleus)

17
Q

Induction

A

Refers to distribution of charge across sigma bonds. Electronegative atoms like more e- around them —> more neg (this less electronegative atoms = more pos)

18
Q

Hybrid orbitals vs sp3 vs sp2 vs sp orbitals

A

Formed by mixing diff types of orbitals vs 1 s orbital + 3 p orbitals = 4 sp3 orbitals, done by putting 1 2s e- into the last unoccupied p space, mostly tetrahedral vs 1 s orbital + 2 p orbitals = 3 sp2 orbitals, alkenes, 120 degrees apart —> max repulsion vs 1 s orbital + p orbital = 2 sp orbitals, alkynes, 180 degrees apart —> linear

19
Q

How to find dipole moment mathematically?

A

p = q*d

p=dipole moment
q=charge
d=displacement vector b/w 2 partial charges

20
Q

Exceptions to e- config

A

4th and 9th column of transition metals can be half filled (ex: 4s13d5 or 4s13d10 as opposed to 4s23d4 or 4s23d9). These exceptions basically have same stability as regular stable e- configs

21
Q

Crystalline lattice

A

Repeating pos and neg ions in a solid state

22
Q

Why is temp necessary for phase change?

A

To overcome intermolecular forces