Acid / base chemistry Flashcards

1
Q

What is an acidulant, and what are some common examples?

A

Acidulants lower the pH of foods and impart a tart taste
-citric acid (most common)
-phosphoric acid (used in cola drinks)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is the equation to calculate pH from [H+]?

A

pH = -log [H+]

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How do strong and weak acids differ in dissociation?

A

Strong Acids: Fully dissociate in water (e.g., HCl)

Weak Acids: Partially dissociate, forming an equilibrium (e.g., acetic acid)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

how is pK calculated? what does the magnitude of numbers indicate?

A

pK = -log Ka

large Ka = small pk = strong acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What does the Henderson-Hasselbalch equation describe?

A

pH= pKa + log [HA] / [A-]

It relates the pH of a solution to the pKa of an acid and the ratio of the conjugate base to the acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what does the final [hydrogen] of a solution depend on?

A

the acids tendency to ionize

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How do titration curves differ for strong acids, weak acids, and polyprotic acids? what equation can be used and when?

A

Strong Acids: Show a sharp pH rise near equivalence

Weak Acids: Show buffering regions near pKa

Polyprotic Acids: Exhibit multiple equivalence points due to successive dissociations

The henderson Hasselbach equation can then be used for weak acid-base systems to calculate pH at any point along the curve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what species reflect what pH for phoshphoric acid?

A

H3PO4 -> H2PO4- : pH = 0-4.7
H2PO4- -> HPO4 2- : pH = 4.7 - 9.7
HPO4 2- -> PO4 3- : pH = 9.7 -14

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What makes a buffer solution effective?

A

A buffer is effective when it consists of a weak acid and its conjugate base (salt), resisting pH changes within a specific range
-acetic acid and sodium acetate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Name examples of food buffers and their pH ranges

A

Citric acid-sodium citrate: pH 2.1–4.7

Acetic acid-sodium acetate: pH 3.6–5.6

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Why is phosphoric acid used in food and beverages?

A

It acts as an acidulant, pH adjuster, and chelating agent
-In cola drinks, it provides a harsh, biting taste

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Which beverages have the lowest pH values, and what is the impact? what is the most common acid added to these drinks?

A

Lemon juice (pH 2.25) and cola drinks (pH ~2.37) are highly acidic, contributing to tooth enamel erosion
-citric acid, phosphoric then malic acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are some common food acidulants and their applications?

A

Citric acid: #1 acidulant, flavor, pH control, chelation

Phosphoric acid: #2 acidulant, soft drinks, pH control, chelation

Lactic acid: Acidulant, preservative

Sorbic acid: Antifungal additive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How is citric acid produced?

A

by the fermentation of molasses by “Aspergillus niger” fungus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What determines the acidity of carboxylic acids?

A

The acidity of carboxylic acids is influenced by the stability of the conjugate base (RCO₂⁻). Greater stabilization increases acidity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How does resonance affect the acidity of carboxylic acids?

A

The conjugate base (RCO₂⁻) is stabilized by resonance, as the negative charge is delocalized between the two oxygen atoms, making the acid stronger

17
Q

which acid would you expect to be the strongest? why?

A

lactic acid
-it has more OH groups which:
1) pulls e- density away from COOH making the H+ on the COOH more positive
2) acidity of the H+ is increase making it easier to dissociate
3) delocalization and reduced e- density stabilizes the conjugate base after proton dissociation

18
Q

How does the inductive effect of -OH groups increase acid strength?

A

The electronegative oxygen in -OH groups pulls electron density away from the acidic proton, increasing its partial positive charge and making it easier to dissociate

19
Q

What are the acid-base properties of ascorbic acid? explain why?

A

Ascorbic acid has two dissociable protons, making it a weak diprotic acid

The first dissociation has a pKa of 4.1, and the second dissociation occurs at a much higher pKa
-the more acidic proton is more easily lost due to the ability to delocalize and stabolize the negative charge

20
Q

What is ascorbic acid, and why is it important?

A

Ascorbic acid (Vitamin C) is a water-soluble vitamin (lactone) that acts as a reducing agent and antioxidant in food and biological systems

21
Q

What are the pKa values of ascorbic acid, and what do they represent?

A

Ascorbic acid has two pKa values:

pKa₁ = 4.1: First proton dissociation

pKa₂ = 11.8: Second proton dissociation

22
Q

What does the Brix measurement represent in food chemistry?

A

Brix measures the percentage of soluble solids (mainly sugars) in a solution, indicating the sweetness of fruit juices and syrups

23
Q

what does the magnitude of values indicate for the brix number?

A

higher values indicate a [higher] of sugar
-flavourful, ripe fruits

lower values indicate [lower] of sugars
-less ripe fruits / diluted solutions

24
Q

How do amino acids behave at low pH? why?

A

At low pH, amino acids are positively charged, with the amino group protonated to form NH3+
-the pka is ~9-11 so a pH below that will mean the group is protonated

25
Explain the relationship between pka and pH? what would you expect of the protonation state depending on the maginitude of each?
when pka > pH = the group is mostly protonate when pka < pH = the group is mostly deprotonated
26
How do carboxylic acids behave at a high pH? why?
at a high pH the COOH group will be deprotonated -the pka ~2-4, so a pH above that would form COO-