Refresher Module Flashcards

1
Q

What is organic chemistry?

A

study of structure, properties, and reaction software ORGANIC COMPOUNDS (carbon containing)

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2
Q

What are hydrocarbons?

A

simplest organic compound containing H + C in single bonds and no functional groups (alkanes and cycloalkanes)

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3
Q

What are functional groups?`

A

group of 1+ atoms whose STRUCTURE gives it particular PROPERTIES + predictable pattern of REACTIVITY

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4
Q

How can functional groups be identified?

A

π-bonds and heteroatoms

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5
Q

What are the 4 types of hydrocarbon functional groups? What are their properties?

A

Alkanes: not reactive bc all C-C and C-H sigma bonds)

Alkenes: contains double bond - π-bonds are weaker than sigma = more reactive = more functional

Alkynes: contains triple bonds (2π)

Aromatics: ring structure of alternative single and double bonds

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6
Q

What are heteroatoms? Why are they important for functional groups?

A

atoms besides H and C

  • heteroatoms have 1+ Lone pairs so electron density around these atoms is different = effects physical properties and reactivity
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7
Q

What determines the intermolecular forces that are in a molecule?

A

structure (controls physical properties) bc of e- distribution

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8
Q

How does the strength of intermolecular forces compare to covalent bonds?

A

weaker than covalent bonds but are collectively strong enough to influence physical properties (melting, boiling points, solubility)

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9
Q

What is ELECTROSTATICS?

A
  • strongest intermolecular force = ionic structures
  • attraction between two molecules of opposite formal charge
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10
Q

What are DIPOLE-DIPOLE INTERACTIONS?

A

attractive force between the NEGATIVE end of a PERMANENT dipole in a molecule & the POSITIVE end of a PERMANENT dipole in another molecule

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11
Q

How does electrostatics and dipole-dipole interactions compare?

A

electrostatics is strongest (formal charge compared to delta + or -)

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12
Q

What is HYDROGEN BONDING? How does it’s strength compare?

A
  • type of dipole-dipole interactions specific to delta + H atom as it is connected to electronegative atom (O or N)
  • stronger type of dipole-dipole interaction because there is a greater difference between the electronegativities
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13
Q

What are hydrogen bonds donors and acceptors?

A

donor: hydrogen
acceptor: other atom H is attracted to

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14
Q

What are Dispersion (London) forces?

A
  • exist in all molecules close to each other
  • temporary dipoles created by electron repulsion
  • weakest
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15
Q

How does the molecule size impact melting and boiling point?

A

longer chain = higher surface area = more intermolecular forces = more difficult to break bonds = higher melting and boiling points

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16
Q

How does the molecule branching impact melting and boiling point?

A

more branching = lower surface area = less dispersion force availability = easier to break bonds = lower melting and boiling points

17
Q

How does ring structure impact melting and boiling point?

A

ring structure = packs well together = increase SA = increase intermolecular forces = more difficult to break bonds = higher melting and boiling points

18
Q

How does the types of bonds generally impact melting and boiling points?

A

highest mp + bp: electrostatic force

h-bonding

dipole-dipole (permanent dipole)

lowest: London forces

19
Q

What is solubility?

A

how well a solute (molecule) dissolves in a particular solvent

20
Q

What is the relationship between the solute and solvent?

A

molecules are most soluble when the types of intermolecular forces are well matched between solute and solvent

21
Q

What are the 3 main solvents?

A
  1. polar protic solvents
  2. polar aprotic
  3. non-polar
22
Q

Wha are POLAR PROTIC solvents?

A

can act as H-bond donors and miscible in water

23
Q

Wha are POLAR APROTIC solvents?

A

strong dipoles

many can act as H-bond acceptors

often highly soluble in water

24
Q

Wha are NON-POLAR solvents?

A

generally held together by dispersion forces

not miscible in water

25
Q

What are the properties/uses of water as a solvent?

A
  • highly polar
  • lab purification
  • adding more non-polar groups decreases water solubility and vice versa
26
Q

hydrophilic?
hydrophobic?

A

hydrophilic: ‘water loving’
- polar enough from favourable intermolecular forces

hydrophobic: “water fearing”
- only London forces
- not string enough to form/overcome intermolecular forces in water

27
Q

How does branching impact solubility?

A

water h-bonds branched molecules better than unbranched (less dispersion forces) = increase solubility

28
Q

How does charge impact solubility?

A

charged molecules interact with water by electrostatics = high reactivity = high solubility

29
Q

formal charge calculations?

A

valence electrons - # bonds on that atom - # unshared e-