#1: Reaction Mechanisms of Organic Molecules Flashcards

1
Q

types of organic molecules reactions

A
  • addition
  • elimination
  • substitution
  • rearrangement
    another: oxidation and reduction
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2
Q

used in a chemical reaction consists of a substrate and reagent

A

reactants

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3
Q

what does a reactant consists

A

substrate and reagent

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4
Q

the reactant that is acted upon or attacked by the reagent

A

substrate

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5
Q

it is the molecule which contains the carbon atom(s) to which bonds are broken and made.

A

substrate

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6
Q

if there is an increase in the number of atoms or groups attached to a carbon(s) in the substrate.

A

addition reaction

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7
Q

an atom or a group of atoms is removed from the substrate, thus there is a decrease in the number of atoms or groups attached to carbon.

A

elimination reactions

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8
Q

when the substrate is transformed into a more unsaturated product

A

elimination reactions

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9
Q

they involve the replacement of an atom or a group of atoms in the substrate by another atom or group of atoms.

A

substitution reaction

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10
Q

reactions involve migration of an atom or group of atoms from one atom to another.

A

rearrangement reaction

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11
Q

occurs when there is an increase in the oxygen content and/or a decrease in the hydrogen content of the substrate.

A

oxidation reaction

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12
Q

there is an increase in the hydrogen content and/or a decrease in the oxygen content of the substrate.

A

reduction reaction

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13
Q

the step by step events by which a substrate is converted to products at a given set of conditions

A

reaction mechanism

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14
Q

are formed in one step and then consumed in a later step of the reaction mechanism.

A

reaction intermediates

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15
Q

The slowest step in the mechanism is called

A

rate determining or rate-limiting step

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16
Q

formed from the transformation of reactants and reagents

A

products

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17
Q

if the covalent bond breaks (covalent fission), what can form?

A

either homolytic or heterolytic cleavage

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18
Q

For a ______ to carbon it can form carbon radical

A

homolytic bond

19
Q

for a ________ it can be a trivalent carbon anion,or carbanions or can be carbon cation or carbocations

A

heterolytic

20
Q

three types of reagents

A
  • nucleophilic (nucleus-loving) or nucleophiles
  • Electrophilic Reagents (electron loving) or electrophiles
  • Radical Like reagents
21
Q
  • usually negatively charged or neutral with a lone pair of electrons.
  • an atom or molecule that in chemical reaction seeks a positive centre, such as the nucleus of an atom.
  • They attack positively charged atoms or low electron density.
A

nucleophilic (nucleus-loving) or nucleophiles

22
Q

Because nucleophiles donate electrons, they are ____.

A

Lewis bases

23
Q

because electrophiles seek an electron pair, they are _____

A

Lewis acids

24
Q
  • they are electron deficient , capable of forming new bonds by accepting a pair of electrons , they attack negatively charged electrons or high electron density.
A

Electrophilic Reagents (electron loving) or electrophiles

25
Q

they have odd number of electrons react easily and attack high electron density atoms.

A

redical like reagents

26
Q

a tertiary radical’s stability is

A

most stable

27
Q

a methyl radical stability is

A

less stable

28
Q

The products formed will undergo reaction intermediates this is the process called

A

reaction mechanisms

29
Q

an electron-poor species (Lewis acid)

A

electrophile

30
Q

an electron-rich species (Lewis base)

A

nucleophile

31
Q

what can be formed when there’s a formation of the covalent bond?

A

homogenic and heterogenic

32
Q

homolytic and homogenic steps are also called

A

radical processes

33
Q

heterolytic and heterogenic steps are also called

A

polar processes

34
Q

reaction intermediates

A

carbanion, carbocations, free radicals

35
Q

steps of reaction mechanism

A

reactants -> intermediate -> product

36
Q

sets of Lewis structures that describe the delocalization of electrons in a polyatomic ion or molecule.

A

resonance structure

37
Q

alternate single and double bonds in an open chain or cyclic compounds results in

A

conjugation

38
Q

The polarity induced in a molecule by the interaction of a lone pair of electrons with a pi bond or the interaction of two pi bonds in nearby atoms

A

resonance effect

39
Q

all nucleophiles are

A

Lewis Bases

40
Q

all electrophiles are

A

Lewis Acids

41
Q

a reagent that is positively charged or electron-deficient species

A

electrophiles

42
Q

a reagent that is negatively charged or electron-rich species

A

nucleophiles

42
Q

a reagent that is negatively charged or electron-rich species

A

nucleophiles