Organic Chemistry and Carbon Bonding Flashcards

1
Q

What is the historical definition of organic chemistry?

A

The chemistry of living things
-compounds obtained from living organisms were thought to poppies vital force that differentiated them from inorganic chemicals

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2
Q

Who synthesised urea from ammonium cyanate?

A

Wohler

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3
Q

What was synthesised in 1958?

A

Synthesis of Perkin’s mauve

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4
Q

What is the modern definition of organic chemistry?

A

The chemistry of compounds of carbon

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5
Q

What forms can organic compounds come in?

A
  • Colourless, coloured
  • Gases, liquids or solds
  • Waxes
  • Plastics
  • Odorous or odourless
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6
Q

Finish the sentence:

If we want to understand life processes on a molecular level we nee to understand the….

A

Structure of organic molecules

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7
Q

What do the properties of organic molecules depends on?

A

Structure of molecule

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8
Q

What is a deoxyribonucleic acid (DNA) relating to organic chemistry?

A

Carbon forms part of the sugar phosphate backbone and the attached bases

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9
Q

What is protein relating to organic chemistry?

A

Carbon forms part of the peptide backbone and attached side chains

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10
Q

What is fatty acids to organic chemistry?

A

Carbon, hydrogen and oxygen containing molecules (Saturated - no double bonds or unsaturated - double C=C bonds)

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11
Q

How are proteins and fatty acids made up by?

A

Biologically catalysed chemical reactions

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12
Q

Fill in the sentence:

Carbon has the ability to bind …. to other elements and for strong bonds with its …..

A

1) Strongly

2) Itself

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13
Q

What does carbon have a rare tendency to do?

A

Catenate

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14
Q

What is meant by catenate?

A

Form chains of carbon atoms

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15
Q

What does the carbon allow being able to catenate?

A

Allows a vast range of structure and therefor properties

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16
Q

What is carbons electron configuration?

A

1s2 2s2 2p2

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17
Q

What does carbon require to have a full valance?

A

4 extra electrons

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18
Q

What are the Lewis structures?

A

Dot and cross structures to display covalent bonding between molecules

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19
Q

What is wrong with the Lewis structure?

A

Does not attempt to explain the geometry of molecules, how bonds are formed or how electrons are shared between atoms

20
Q

Define atomic orbital:

A

Region within an atom which can hold up to two electrons with opposite spins

21
Q

What are the 4 meaningful types of orbitals?

A

s, p, d or f

22
Q

Finish the sentence:

Each orbital has a…

A

specific shape

23
Q

What are orbitals arranged into?

A

Groups of similar energies

24
Q

What is principle quantum number (n)?

A

Related to the energy of an orbital

25
Q

What is molecular orbital theory?

A

Two half-filled atomic orbitals combine to give a single or s-bond (sigma) consisting of two s-molecular orbitals

26
Q

What does a double bond consist of?

A

s-bond and a p-bond

27
Q

What does a molecular orbitals with double bonds form?

A

-Two p orbitals can overlap end-on, to form two s-molecular orbitals
OR
-Two p orbitals can overlap side-on, to form two p-molecular orbitals

28
Q

What is the ground state?

A

The lowest state

29
Q

If a carbon was to remain at a ground stat in a molecule it must:

A
  • Share two electrons

- Only have 6 electrons in its valance orbital

30
Q

1s atomic orbital + 2s atomic orbital =

A

Have correct symmetry to form sigma bond

31
Q

1s atomic orbital + 2px orbital =

A

Have the correct symmetry to form a sigma bond

32
Q

1s atomic orbital + 2py orbital =

A

Do no have the correct symmetry

33
Q

What is the hybrid model?

A

Mathematically, energetically favoured in the resting molecular compound

34
Q

What is orbital hybridisation?

A

2s orbital and 2p orbitals are mixed to give sp3 hybrid orbitals

35
Q

What does it mean if orbital hybridisation happens?

A

Carbon can form 4 covalent bonds to fulfil the octet rule

36
Q

What happens in methane relating to hybrid orbitals?

A

Sp3 orbitals mixes with hydrogen s orbital to form 4 sigma bonds to four hydrogen atoms

37
Q

What is the bond angle in methane?

A

109.5 bond angle

38
Q

Why does a tetrahedral arrangement occur?

A

Mutual repulsion will push the molecular orbitals as far apart as possible

39
Q

Describe ethane in relation to hybrid orbitals:

A
  • Three sp3 orbitals mix with the s orbitals of three hydrogen atoms to from three sigma bonds
  • One sp3 orbital mixes with an sp3 orbital from second carbon atom forming c-c sigma bond
40
Q

How do you achieve double carbon bond?

A

Having three sp2 hybrid orbitals and one unhybridized p orbital

41
Q

What is an sp2 orbital hybridisation?

A

One s orbital and two p orbitals

42
Q

Describe ethene in terms of orbital hybridisation:

A

Each carbon atom forms three sigma bonds:

  • 2 to two hydrogen atoms
  • 1 to second carbon atom (causing an overlap of sp2)

Each carbon atom forms a pie bond to the second carbon atom (overlap of unhybridized p orbitals)

43
Q

Which bond is stronger sigma or pie bond?

A

Sigma

44
Q

Describe sigma bond:

A
  • End-on overlap (more effective)
  • 346 Kjmol^-1
  • Stronger
  • Less reactive
45
Q

Describe pie bond:

A
  • Edgewise overlap (less effective)
  • 252 KJmol^-1
  • Weaker
  • More reactive
46
Q

How do you achieve a triple carbon bond?

A

2x sp hybrid orbitals
2x unhybridized orbitals
p orbital define the geometry around the carbon atom and the others try and position as far as possible
-one sigma bond
-2 pie bonds (overlap of unhybridised p-orbitals)