Study Guide 3: Introduction to Reaction Mechanisms Flashcards

1
Q

π bonds are easily broken and make a __________, a _______, and a ___________

A

molecule
base
nucleophile

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2
Q

It is an atom or group of atoms with characteristic chemical and physical properties – the reactive part of the molecule

A

Functional Group

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3
Q

indicates how the energies of the reactants, products, and intermediates compare

A

energy diagram

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4
Q

refers to the bond dissociation energy when measured under standard conditions

A

ΔH ̊

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5
Q

hv

A

indicates light is needed

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6
Q

Ea

A

activation energy

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7
Q

gives us a clue to the general type of reaction a particular class of compound undergoes

A

Reactive Sites

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8
Q

The energy required to break a bond via homolytic bond cleavage

A

Bond Dissociation Energy

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9
Q

are easily broken and make a molecule, a base, and a nucleophile

A

π bonds

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10
Q

indicates how readily a reaction proceeds

A

energy diagram

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11
Q

energy needed to break bonds in the reactants

A

Activation Energy

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12
Q

one replaces the other, for saturated compounds

A

Substitution

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13
Q

What are the four types of organic reactions?

A

addition
rearrangement
elimination
substitution

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14
Q

What are the three common types of functional groups?

A

Hydrocarbons (C-C and C-H)
Compounds containing C-Z σ bond (where Z – electronegative elements)
Compounds containing a C=O group

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15
Q

Bond Dissociation Energy is energy required to break a bond via?

A

homolytic bond cleavage

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16
Q

It will start with functional groups, looking for electron-rich and electron-deficient sites, and bonds that might be broken easily

A

Organic Reactions

17
Q

(-)ΔH ̊

A

exothermic reaction

18
Q

molecules undergo reorganization of its constituent parts

A

Rearrangement

19
Q

characteristics of compounds with multiple bonds

A

addition

20
Q

is the energy difference between reactants and products

A

ΔH ̊

21
Q

Low Ea

A

fast reaction

22
Q

Δ

A

indicates heat is added

23
Q

opposite of addition

A

Elimination

24
Q

It is a schematic representation of the energy changes that take place as reactants are converted to products

A

Energy Diagram

25
Q

indicates how many steps are involved

A

energy diagram

26
Q

It is caused by the presence of heteroatoms having lone pairs and electron deficient sites on carbon

A

Reactivity

27
Q

What are the different common bonds?

A

bonds to H
C-C bonds
bonds to methyl
X-X bonds