3. Bonding Flashcards

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1
Q

sigma bond vs pi bond

A

single bonds; allows free rotation around axis vs double and triple bonds; doesn’t allow free rotation around axis

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2
Q

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

A

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

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3
Q

Tetrahedron has what type of orbitals? What about alkenes? What about a triple bond or 2 adjacent double bonds?

A

sp3; sp2 120 degrees; sp 180 degrees

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4
Q

Which elements do H bonds?

A

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

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5
Q

What does increased branching do to bpt vs mpt?

A

Lowers it vs lowers it UNTIL BRANCHING BECOMES MORE SYMMETRICAL –> RAISES IT

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6
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-

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7
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 signs of 2 atomic orbitals that are different

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8
Q

Principal vs azithumal/angular momentum vs magnetic vs spin quantum number

A

Energy level/shell, n, max # of e- w/in a shell: 2n^2 vs subshell, l, max # of e- w/in a subshell: 4l + 2, ranges from 0 to n-1 (ie. In the first shell, you have one subshell which is l=0; in the second shell, you have two subshells which are l=0 and l=1; etc); energy of subshells inc with increasing l values (ex: 3d has more energy than 4s) vs # of orbitals, ranges b/w l and -l including 0 vs spin and momentum, either +1/2 or -1/2

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9
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)

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10
Q

Hybrid orbital vs sp3 orbital vs sp2 orbital vs sp orbital

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, 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

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11
Q

Molecular orbitals contain how many max numbers of e-?

A

2 e- (remember: Pauli exclusion principle)

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12
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)

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13
Q

Characteristics of aromatic cmpds

A

Nonpolar/Hydrophobic, inc acidity b/c they stabilize neg charges, cyclic, stable, planar, conjugated all around, Huckel’s rule: 4n+2 pi e- where n=any integer

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14
Q

Hydrogenation of alkenes into alkanes involve what?

A

A metal catalyst

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