Honors Chemistry- Buffers and Titrations

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54 Terms

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What is the role of a buffer?

Resists change in pH

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Contents of a buffer?

Weak acid and it’s conjugate base

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How do you make a buffer?

Combine a weak acid and it’s conj base from separate solutions

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Will putting a weak acid in water work?

NO

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How does a buffer acid resist pH change?

Reacts with added OH-

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How does a buffer base resist pH change?

Reacts with added H+

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Buffer capacity

How good a buffer is at neutralizing added H+ or OH-

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Buffer better at neutralizing acid or base when HA > A-?

Better at neut added OH-, because more buff acid

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Buffer better at neutralizing acid or base when HA < A- ?

Better at neut. added H+, because more buff base

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What is special about the pH of a buffer?

It is close to the pKa and higher or lower based on concentrations

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Henderson-Hasselbach Equation

pH = pKₐ + log([A⁻]/[HA])

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Henderson-Hasselbach Equation, IMPORTANT RULE!!!!

The concentration of the conj BASE goes on top, and the concentration of an acid is on the bottom

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pH and pKa relationship: (HA)=(A-)

pH=pKa

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pH and pKa relationship: (A-) > (HA)

pH>pKa

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pH and pKa relationship: (HA) > (A-)

pH<pKa

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How to do engineering with a buffer?

Pick an acid with a pKa closest to the desired pH. For example, if you want a buffer with a pH of 5.15, the pKa is around 5, so find one raised to the -5, if not, the next best option is to go to a higher negative, so -6

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What to do if the engineered buffer is too concentrated?

Multiply both top and bottom by 0.1 until a desired concentration is met

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Equivalence point

the “end pt” where only products are present, the indicator is picked based off this point too

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What is important about the titration problem set up?

The wording will equal the order! First one listed is in the FLASK, and second one listed is in the burette

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SA+SB titration: Point A

Before the base is added, there is only strong acid in the flask

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SA+SB titration: Point A: Solve for pH

Take the negative log of the concentration of (HX), by doing an ice problem and writing the chemical rxn out

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SA+SB titration: Point B

Where some base is added, and in the flask there starts to form a buffer.

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SA+SB titration: Point B: Solving for pH

Use stoich to find the concentration of H+ left, then take the negative log of H+

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SA+SB titration: Point C

Enough base is added to reach the eq point, so there are only products left

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SA+SB titration: Point C: Solving for pH

It is 7!

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SA+SB titration: Point D

Base is continued to be added, there is no more strong acid left, but rather a reactant of the strong base is now there with the buffer as a product

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SA+SB titration: Point D: Solving for pH

Use stoich to find the (OH-) left, and then take the -log of OH, then subtract 14 to get pH

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WA+SB titration: Point A

Before adding base, there is weak acid in the flask.

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WA+SB titration: Point A: Solving for pH

In order to find the pH, you must solve for Ka, and then take the -log of the H+ concentration to find the pH

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WA+SB titration: Point B

Some of the base is added, which will form the weak acids conjugate base.

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WA+SB titration: Point B: Solving for pH

Use stoich to find the concentration and then use the buffer equation pH = pKₐ + log([A⁻]/[HA])

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WA+SB titration: Point C

Enough base is added to reach eq point, meaning there are only products left

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WA+SB titration: Point C: Solving for pH

Use stoich for the concentration, and then plug that into a Kb equation, and take the -log of (OH-) and subtract 14 to get your pH

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WA+SB titration: Point D

Base contiunes to be added, leaving the strong base as a reactant, and products are intact

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WA+SB titration: Point D: Solving for pH

Stoich for the concentration of (OH-), and take the -log of (OH-) and subtract 14 to get pH

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SA+WB titration: Point A

Before acid is added, there is still weak base in the flask

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SA+WB titration: Point A: Solving for pH

Find your Kb, and then take the -log of (OH-) and subtract 14 to get pH

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SA+WB titration: Point B

Some of the weak acid is added, which starts to form the products and the buffer

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SA+WB titration: Point B: Solving for pH

Stoich to find concentration, and then use the buffer equation to find pH pH = pKₐ + log([A⁻]/[HA])

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SA+WB titration: Point C

Enough acid is added to reach the eq point, so there are only products left

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SA+WB titration: Point C: Solving for pH

Stoich to find the concentration, and then find the Ka and use that H+ concentration to take the -log of it to obtain pH

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SA+WB titration: Point D

Acid will continue to be added, leaving only the strong acid as a reactant and the product

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SA+WB titration: Point D: Solving for pH

Use stoich to find the H+ concentration and take the -log of H+

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Under the eq point, what does it establish on the x-axis?

X amount of titrant added

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Under the point ½ less than the eq point, what does it establish on the x-axis, and what can we call this point?

½ x. the ½ equiv. volume

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What is special at the ½ equiv. volume point?

pH=pKa, where (HA)=(A-)

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If the equivlance point is greater than 7, there is more…

Buffer base

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NEVER ASSUME THAT THE EQ POINT IS

7

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What two points can the ½ eq point form?

It can be in between point X and point Y, where point Y is always closer to the eq point, this is known as the buffer zone

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On an ascending pH graph, what is the buffer zone relationship between X and Y?

X: pH<pKa

y: pH>pKa

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On an descending pH graph, what is the buffer zone relationship between X and Y?

X: pH>pKa

Y: pH<pKa

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