3.2 Synthesis Flashcards

1
Q

Fission

A

Process of bond breaking

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2
Q

Homolytic Fission (3 points)

A
  • Results in the formation of two neutral radicals
  • Occurs when each atom retains one electron from the sigma covalent bond and the bond breaks evenly
  • Normally occurs when non-polar covalent bonds are broken
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3
Q

Heterolytic Fission (3 points)

A
  • Results in the formation of two oppositely charged ions
  • Occurs when one atom retains both electrons from the sigma covalent bond and the bond breaks unevenly
  • Normally occurs when polar covalent bonds are broken
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4
Q

Single-Headed Arrow

A

Movement of a single electron

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5
Q

Double-Headed Arrow

A

Movement of an electron pair

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6
Q

Homolytic fission in terms of arrows

A

Two single-headed arrows starting at the middle of a covalent bond

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7
Q

Heterolytic fission in terms of arrows

A

One double-headed arrow starting at the middle of a covalent bond

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8
Q

Nucleophiles (3 points)

A
  • Negatively charged ions or neutral molecules that are electron rich
  • Attracted towards atoms with a partial or full positive charge
  • Able to donate an electron pair to form a new covalent bond
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9
Q

Examples of Nucleophiles

A

Cl-, Br-, OH-, CN-, NH3 and H2O

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10
Q

Electrophiles (3 points)

A
  • Positively charged ions or neutral molecules that are electron deficient
  • Attracted towards atoms with a partial or full negative charge
  • Able to accept an electron pair to form a new covalent bond
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11
Q

Examples of Electrophiles

A

H+, NO2+, SO3

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12
Q

Haloalkanes

A

Substituted alkanes in which one or more of the hydrogen atoms is replaced with a halogen atom

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13
Q

Monohaloalkanes (2 points)

A
  • Contain one halogen atom
  • Can be classified as primary, secondary or tertiary with number of alkyl groups
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14
Q

Alcohols

A

Substituted alkanes in which one or more of the hydrogen atoms is replaced with a hydroxyl functional group

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15
Q

Ethers

A

Substituted alkanes in which a hydrogen atom is replaced with an alkoxy functional group, -OR

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16
Q

SN1 Reactions

A

Nucleophilic substitution reaction with one species in the rate determining step and occurs in a minimum of two steps via a trigonal planar carbocation intermediate

17
Q

SN2 Reactions

A

Nucleophilic substitution reaction with two species in the rate determining step and occurs in a single step via a single five-centred, trigonal bipyramidal transition state

18
Q

Substitution

A

Atoms are added to a molecule by replacing atoms already present

19
Q

Addition

A

Joining two or more molecules together to form a larger molecule

20
Q

Elimination

A

When a small group of atoms breaks away from a larger molecule with the release of a small molecule

21
Q

Condensation

A

The joining of molecules with the release of water as a product

22
Q

Hydrolysis

A

The breakdown of a molecule by water

23
Q

Neutralisation

A

When an acid and a base react to form water

24
Q

Markovnikov’s Rule

A

States that when a hydrogen halide or water is added to an unsymmetrical alkene, the hydrogen atom becomes attached to the carbon with the most hydrogen atoms attached to it already.

25
Q

Amines

A

Organic derivatives of ammonia in which one or more hydrogen atoms of ammonia has been replaced by an alkyl group

26
Q

Reducing Agent Example

A

Lithium Aluminium Hydride