Lecture 1 book recap Flashcards

(32 cards)

1
Q

how do you calculate the dipole moment?

A

the size of the charge x the distances between the charges with a si unit of D (debye) which is to the power of -18

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2
Q

1A is = to

A

1 x 10^-8

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3
Q

what are electrostatic potential maps

A

it is a model that shows how charge is distributed in the molecule under a map and therefore shows to which degree a molecule attracts the other molecules

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4
Q

what do the colours on the electrostatic map show

A

red signifies the region with the most negative electrostatic potential

Blue signifies the region with the most positive electrostatic potential

then from orange to yellow to green is the middle between red and blue from orange being more negative the yellow and green

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5
Q

the size of the electrostatic potential map shows?

A

the electron denisty of the molecule

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6
Q

formal charge =

A

number of valence electrons - (number of bonds + number of lone pairs)

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7
Q

what is the probability of finding the electron in 2s orbital

A

usually, it would be more than 90% but due to the wave-like property of the electron it will form a standing wave with nodes and anti-nodes where the anti-nodes would have a probability of zero to find it

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8
Q

when two orbitals join in a sigma bond what happens to the energy

A

energy is released as the electrons in the orbitals are attracted to their own nucleus and to the nucleus of the other orbital

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9
Q

what is bond dissociation energy

A

the energy required to break a bond, or the energy released when the bond is broken

(very covalent bond has a specific bond length and bond dissociation energy)

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10
Q

when two orbitals form a sigma bond they form a new molecular orbital, and that is due to?

A

the wave-like behavior of electrons the two orbitals can constructively interfere.

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11
Q

The constructive combination of two s atomic orbitals is called a

A

a sigma bonding molecular orbital

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12
Q

The destructive combination
of two s atomic orbitals is called

A

S* antibonding molecular orbital where to reaction happens

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13
Q

what binds the molecular orbitals

A

the electrons in the middle between the two nuclei can freely attract both nuclei, and this increase in electron density and keeps the nucleus bonded and have low energy making it stable

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14
Q

how do some molecular orbitals not bond

A

because the electrons are not found anywhere between the nuclei because of the nodal plane, this leaves the positive nuclei exposed to each other causing them to repulse each other and have very high energies making it unstable

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15
Q

the covalent bond strength increases as the

A

as the atomic orbital overlap increases

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16
Q

what is a sideway deconstructive overlap between two p orbitals

A

pi* antibonding molecular orbital which has two nodal planes

17
Q

which is stronger C=C or C-C

18
Q

where are the high electron density regions in ethyne C≡C and why

A

in the front, back, top, and bottom of the molecule as the two unhybridized orbitals are perpendicular to each other (to minimize repulsion) so they side way overlap

19
Q

which is stronger C≡C or C=C

A

C≡C because it is held by 6 electrons

20
Q

what are the three reasons carbon might form 3 bonds

A
  1. it has a positive charge (it forms 3 hybridized orbitals of 1 s and 2 p forming 3 covalent bond with the 3rd p being empty and perpendicular
  2. it has a negative charge (it forms 3 hybridized orbitals of 1 s and 2 p forming 3 covalent bonds with the p orbital have an unpaired electron whose electron density is split between the two lobs (50%-50%)
  3. It has one unpaired electron (radical) (it forms 4 hybridized orbital os 1s and 3 p with 3sp^3 forming bonds with hydrogen and one sp^3 having a lone pair causing all the orbital to move very far away from it to form an angle of 107.3 trigonal pyramidal)
21
Q

how does Nitrogen form 3 bonds

A

nitrogen has 3 lone pairs in its p orbital which can explain how it forms 3 covalent bonds which should form 90* but when observed ammonia forms a bond angle of 107.3 which can only be explained by the fact that ammonia has 4 hybridized sp^3 orbital at which 3 of of them form covalent bonds and one of them would have a lone pair which has a larger election density than the rest of the sp^3 orbitals (when the join with hydrogen) so they are used to an angle of 107.3

22
Q

ammonium ion forms a bond angle of

A

109.5 because all the N-H bonds are the same and there are no lone pairs

23
Q

how does oxygen form 2 bonds

A

oxygen has two lone electrons in its valence shell so it is expected that it forms two covalent bonds but from data, we see that water has an angle of 104.5 and that can be explained by the formation of 4 hybridized orbitals of sp^3 with 2 having one election and being used for bonds and the other two having a lone pair in there sp^3 orbital and this causing so much repulsion forming the bond angle of 104.5 (v-shaped)

24
Q

what is bonding like in HX

A

so halides have only one lone electron in their valence shell so it forms only one bond so due to that we can figure out the bond angle it forms but we do know that the 3 lone pairs of electrons are very energetically similar and want tp minimize repulsion which indicates that X forms 4 hybridized sp^3 orbitals with 3 of them having a lone pair and one of then having an electron reading for covalent bonding so HX is due to the overlap of 1sp^3 and s from hydrogen

25
explain the rs between orbital overlap and halogen size
so as the orbital overlap decreases the halogen size increases that is because as we go down the halide group the sp^3 hybridized orbital becomes from further shells (f - 2, cl-3) so less electron density as they become further from the nucleus ( so the HX becomes longer and weaker)
26
when we have more than one dipole in a molecule what determines the overall dipole
the magnitude and direction of the individual bond angles ( the vector sum)
27
what is hyperconjugation.
the delocalization of electrons by the overlap of a sigma orbital with a empty orbital
28
In Newman projection the carbon with less different groups is
placed in the back
29
The degree of rotation of each conformer is identified
a dihedral angle - the angle formed in Newman projection form a bond formed in the font carbon and a bond formed in the back carbon
30
what anti and gauche conformer
anti conformer is the one with the least steric strain and gauche are the ones that are staggered but have more strain than anti (they usually have the same energy level)
31
the steric strain that gauche experience are called
gauche interactions
32