Organic Chemistry Flashcards

1
Q

How many valence electrons does carbon have?

A

4

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2
Q

What is carbons electron configuration? And its valence shell configuration?

A

1s2, 2s2, 2p2

Valence shell = 2s2, 2p2

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3
Q

What is carbons electronegativity number?

A

2.5

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4
Q

Which element has the highest electronegativity and what is it?

A

Fluorine

4

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5
Q

What bond type does carbon have? What are the pros of this?

A
4 Covalent (between atoms with equal negativity)
And 4 polar covalent (atoms with differing electronegativity) 
Means carbon can bond to other atoms in a lot of different combinations and form many different types of structures
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6
Q

What is the empirical formula?

A

The simplest while number ratio of elements

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7
Q

What is the molecular formula?

A

The actual number of atoms of each element

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8
Q

What is the structural formula?

A

Minimal detail for an unambiguous structure

Writes out every compound in molecule

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9
Q

What is the displayed formula

A

Relative placing of atoms and bonds between them (diagram)

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10
Q

What is the skeletal formula

A

The carbon skeleton and functional groups only (very basic diagram)

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11
Q

Describe sigma bonds

A

When 2 orbitals overlap as 2 atoms approach
End to end overlap bond formed = sigma
Electrons of one atom attracted to nucleus of the other
Attraction continues until repulsion between the 2 nuclei outweighs it

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12
Q

What’s is hybridisation?

A

Combining 2+ atomic orbitals from the same atom to create new orbitals

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13
Q

Describe sp3 hybridisation

A

S and p orbitals are mixed to form hybrid orbitals

1 s and 3 p orbitals are mixed (a 2s electron prompted into empty 2p orbital = 4 unpaired electrons)

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14
Q

Describe sp2 hybridisation

A

One s orbital and two p orbitals hybridise and form sigma bonds (one p orbital left over)
Sp2 hybridisation gives a bond angle of 121.3 degrees
The 2 pure p orbitals of the 2 carbon atoms can overlap sideways to form a pi bond

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15
Q

What is a pi bond

A

covalent chemical bonds where two lobes of an orbital on one atom overlap two lobes of an orbital on another atom and this overlap occurs laterally

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16
Q

Describe benzene structure

A
  • planar molecule
  • each carbon is sp2 hybridised
  • 6 electrons in pure p orbitals capable of overlapping
  • get delocalisation over the ring
17
Q

Describe sp hybridisation

A
  • 2 pure p orbitals left over per carbon atom = 2 pi bonds
  • 1s atom and 1p atom hybridise
  • each carbon atom forms 2 sigma bonds and 2 pi bonds
18
Q

What are the properties of organic compounds? (4)

A
  • physical and chemical behaviour heavily influenced by molecules polarity
  • most are not soluble with water
  • somewhat soluble if have oxygen or nitrogen atoms: electronegative atoms form hydrogen bonds with the water
  • many undergo combustion and burn vigorously in air
19
Q

Describe polarity of organic molecules

A
  • covalent bond between 2 carbons non polar because electrons shared equally
  • most elements found in organic compounds more electronegative than carbon (except H)
  • polarity of molecule determined by polarity of bonds and structure
  • bond can be polar but molecule non polar if has symmetrical arrangement of polar bonds that cancels out the dipoles.
20
Q

What are the 2 classes of organic compounds

A

-aromatic
Contains cyclic conjugated (alternating double and single bonds) double bond system with 4n + 2pi electrons

-aliphatic
All other compounds without a ring system

21
Q

Why do we have classes of organic compounds

A
  • there are millions of different types
  • characteristic structural features ‘functional groups’
  • allows to classify and name compounds within families
  • identification of functional groups helps to predict reactivity of a compound
22
Q

Oxidation of carbon

A

They form additional bonds to oxygen

23
Q

Reduction of carbon

A

They form additional bonds to hydrogen

24
Q

Substitution

A

Exchange of one atom in a molecule with another atom/group of atoms

25
Q

Elimination

A

Single reactant split into 2 products

26
Q

Addition

A

2 reactants add together to form single product

27
Q

Homolytic reaction of carbon compound

A
  • 1 electron transferred to each atom

- formation of radicals

28
Q

Heterolytic reaction of carbon compound

A
  • 2 electrons transferred to another atom

- formation of ions

29
Q

What is a radical?

A

Atom containing at least 1 unpaired electron