Chapter 2: 2.1 Acid/Base Equilibrium Fundamentals Flashcards

1
Q

Why doe we use acids in organic chemistry?

A

Bronsted-Lowry acids are sources of protons
* Are key catalysts in a number of organic transformations
* Less reactive functional groups are converted to more reactive/electrophilic functionalities by addition of strong acid

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2
Q

Why do we use bases in organic chemistry?

A

Bronsted-Lowry bases are proton acceptors
* Used to deprotonate compounds
* Results in more nucleophilic anions and can form new bonds
* Key step in many carbon-carbon bond forming reactions

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3
Q

What is a defining characteristic of Bronsted-Lowry Acids and Bases?

A

They exchange protons (H+)

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4
Q

Define:

Bronsted-Lowry Acid

A

A proton donor

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5
Q

Define:

Bronsted-Lowry Base

A

A proton acceptor

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6
Q

When a Bronsted-Lowry acid and base react together, what happens?

A
  • The acid will form a conjugate base
  • The base will form a conjugate acid
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7
Q

What is a characteristic of Arrhenius acids and bases?

A

They do chemistry in aqueous (water) solution

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8
Q

Define:

Arrhenius Acid

A

A proton donor

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9
Q

Define:

Arrhenius Base

A

A hydroxide donor

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10
Q

True or False:

The definitions for Arrhenius Acids and Bases are out of date and not used anymore

A

True

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11
Q

What is a characteristic of Lewis Acids and Bases?

A

They are electron donors and acceptors; it is for this reason that this definition is less common in organic chemistry

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12
Q

Define:

Lewis Acid

A

An electron pair acceptor

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13
Q

Define:

Lewis Base

A

An electron pair donor

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14
Q

What is used to quantify the strength of an acid?

A

Ka and pKa values

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15
Q

What is the general K expression?

A

K = [Products] / [Reactants]

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16
Q

Less generally, what is the formula for Ka?

A

Ka = [H+][A-] / [HA]

17
Q

What is the formula for pKa?

A

pKa = -log (Ka)

18
Q

As Ka goes up, pKa goes —- and acidity goes –

A
  • Down
  • Up