Basic Introduction II Flashcards

This study section includes Formal Charge, Lewis Structure of Organic Compounds, Organic Molecules Representation, and Hybridization

1
Q

Determines the best Lewis Dot Structure of a molecule

A

Formal charge

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2
Q

Where is the site of chemical reactivity?

A

Location of charges

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3
Q

The equation of Formal charge

A

FC = “should” - “has”

should = group no.; has = directly attached to the atom

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4
Q

What?

A carbon with positive charge

A

Carbocation

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5
Q

What?

A carbon with negative charge

A

Carbanion

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6
Q

What?

A carbon with lone pair of electron

A

Carbon radical

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7
Q

How many covalent bond?

X (halogens)

A

One (1)

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8
Q

How many covalent bond?

N (Nitrogen)

A

Three (3)

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9
Q

How many covalent bond?

C (Carbon)

A

Four (4)

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10
Q

How many covalent bond?

O (Oxygen)

A

Two (2)

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11
Q

How many covalent bond?

H (Hydrogen)

A

One (1)

based on duet rule

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12
Q

Trivia/Compound

It is also called as fruit ripening carbon

A

Ethylene

Formula: C2H4

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13
Q

Trivia/Compound

Used as refrigerant

A

flouromethane

Formula: CH3F

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14
Q

Trivia/Compound

Used as a precursor for illegal drugs “shabu”

A

methylamine

Formula: CH3NH2

Reductive Amination

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15
Q

How to determine if the Lewis Structure of a molecule is correct?

A

Check the formal charge and if following the octet rule

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16
Q

What is the angle in a single bond carbon?

A

109.5

tetrahedral

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17
Q

Structure Recall

In plane of paper

A

Line

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18
Q

Structure Recall

Going INTO the paper (away from you)

A

Dash

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19
Q

Structure Recall

Coming OUT of the paper (towards you)

A

Wedge

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20
Q

What is the angle?

Double bonds

A

120

Planar

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21
Q

Trivia/Compound

Component of rubber latex

A

Isoprene

Hevea brasiliensis

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22
Q

How to determine the number of hydrogen bonded to a carbon?

A

4 - (# of bonds attached to C)

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23
Q

What is the angle?

Triple Bonds

A

180

linear

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24
Q

What are the 3 hybrid orbitals?

A

sp3, sp2, sp

25
Mixing of atomic orbitals to form newly hybridized orbitals influencing molecular geometry and bonding properties.
Orbital hybridization
26
What is the electron configuration of Carbon?
[He]2s2 2p2
27
Electron orbitals that have the same energy level
Degenerate orbitals
28
What is the principle of hybridization?
Mixing of two orbitals | Which consist of the valence electrons
29
Hybrid orbitals can also be called?
Degenerate orbitals
30
# True or False? The energy level of the hybrid orbitals should be *between* the their original energy levels.
True
31
If there are 4 atomic orbitals, how may hybrid orbitals should be generated?
4 hybrid orbitals
32
# In 2sp3 What does '2' signifies?
Principal Energy Level
33
# In 2sp3 What does 's' signifies?
From 2s orbital participating in the hybridization
34
# In 2sp3 What does 'p' signifies?
From 2p orbital participating in the hybridization
35
# In 2sp3 What does '3' signifies?
no. of 2p orbital used in hybridization
36
What is the shape of s orbital?
Sphere
37
What is the shape of p orbital?
dumbell shape
38
What is the bond formed by the HEAD-ON overlap of atomic orbitals and hybrid orbital?
Covalent sigma bond
39
Bond that allows free rotation
Sigma bond
40
Covalent bond formed from SIDEWAYS overlap of Unhybridized p-orbitals
Pi bond
41
What is the hybridization of ethene? | C2H4
sp2
42
One p-orbital and its electron will be saved in the side to create a ____?
Pi bond ## Footnote Hybridization Part 3 by Sir Maki
43
What is included in the determination of shape of molecule?
Hybrid orbitals | Unhybridized is neglected
44
# True or False? The C-C double bond in C2H4 is a sigma bond formed from C(sp2) - C(sp2) orbitals and a pi bond formed from unhybridized p orbitals
True
45
# True or False? Free rotation is ALLOWED in pi bonds
**False**. NOT Allowed | The parallel overlapping of unhybridized orbitals should be maintained.
46
# True or False? Geometric isomers exist in double bonds.
True
47
How many orbitals are saved to create two pi-bonds in triple bonded molecule?
Two (2) p-orbitals
48
# True or False? The naming of hybrid orbitals (sp3, sp2, sp) is based on degenerate orbitals
True | Unhybridized orbitals for non-single bonds are saved to create pi-bonds.
49
Where are the lone pairs located in hybridization?
Hybridized orbital (2 full spins)
50
# Yes or No? Does lone pair affect the geometry of the molecule?
Yes | The angle is now lesser.
51
Shape that has 107 deg
Trigonal pyramidal
52
The effect of lone pair of electrons is described in what theory?
Valence Shell Electron Pair Repulsion (**VSPER**) Theory | Gillespie-Nyholm Theory
53
What is the formula of Steric No. (SN)?
SN = sum of attached atoms + lone pairs | SN is used as shortcut method to determine the hybridization
54
# If SN is 4
sp3
55
# If SN is 3
sp2
56
# If SN is 2
sp
57
An OTC pain reliever
Ibuprofen
58
# Exemption in hybridization If the lone pair is adjacent to pi bond, they tend to be part of unhybridized obrital instead of degenerate. Why? | Principle of resonance structure
Delocalization of lone pair | Creating pi-bond system, instead ## Footnote Hybridization Part 8 by Sir Maki
59
What is unhybridized orbital of Carbon (C) atom?
2p | Hybridization Part 9 by sir Maki