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Reading Time: 6 min
Last Updated: February 10, 2026
Main Ideas: 4
Reading Time: 6 min
Last Updated: February 10, 2026
Main Ideas: 4

Topic 3.7 Notes – Solutions and Mixtures

Verified for 2027 AP® Chemistry Exam
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Topic 3.7 covers what solutions are, how they differ from other mixtures, and how we describe their composition using molarity. You’ll connect the particle-level picture of dissolving to the math used in lab calculations and dilution problems.

What Solutions Are

A solution is a homogeneous mixture. That means its macroscopic properties (color, density, concentration) are the same everywhere in the sample.

A heterogeneous mixture has visibly or measurably different regions. The properties depend on where you sample.

Here’s the visual difference:

Study guide illustration

Homogeneous vs. heterogeneous mixtures

In the left beaker, the mixture looks uniform throughout. In the right beaker, you can clearly see different pieces and regions. If you scoop from the top or bottom of a homogeneous solution, you get the same composition. With a heterogeneous mixture, you might not.

Parts of a Solution

  • Solute → the substance being dissolved (usually smaller amount)
  • Solvent → the substance doing the dissolving (usually larger amount)
  • Aqueous (aq) → solution where the solvent is water

Example: In NaCl(aq)\ce{NaCl(aq)}, water is the solvent and sodium and chloride ions are the solute particles.

Solutions Can Exist in Any Phase

“Solution” does not mean liquid.

  • Solid solutions → alloys like steel (iron + carbon)
  • Liquid solutions → salt water, ethanol in water
  • Gas solutions → air (mostly NX2\ce{N2} with OX2\ce{O2}, COX2\ce{CO2}, etc.)

The key is uniform composition, not phase.

How Solutions Form at the Particle Level

When something dissolves, particles rearrange. Intermolecular forces (IMFs) are broken and formed.

Three energy-related steps happen:

  1. Separate solute particles (break solute-solute attractions)
  2. Separate solvent particles (break solvent-solvent attractions)
  3. Form solute-solvent attractions

This overall process is called solvation.

If the solvent is water, it’s called hydration.

For example, when NaCl\ce{NaCl} dissolves:

  • The ionic lattice is broken apart.
  • Water molecules separate slightly.
  • Water surrounds NaX+\ce{Na^{+}} and ClX−\ce{Cl^{-}} ions.
Study guide illustration

Hydration of NaCl in water

Notice the orientation of the water molecules. The partially negative oxygen atoms point toward NaX+\ce{Na^{+}}, and the partially positive hydrogen atoms point toward ClX−\ce{Cl^{-}}. That orientation reflects ion-dipole attractions forming during hydration.

A solution forms when the new solute-solvent attractions are strong enough to compensate for what was broken. On exams, you’ll often explain dissolving in terms of IMF changes, not just “it mixes.”

Expressing Concentration with Molarity

Concentration tells you how much solute is present in a given amount of solution.

The main unit you need is molarity (M):

M=moles of soluteliters of solution M = \frac{\text{moles of solute}}{\text{liters of solution}}

Units are mol/L.

Two details students miss:

  • The numerator is moles of solute only.
  • The denominator is total volume of the solution, not just solvent.

Rearranged Forms

moles=M×V \text{moles} = M \times V

V=molesM V = \frac{\text{moles}}{M}

Volume must be in liters.

Quick Example

Suppose you dissolve 0.75 mol of KNOX3\ce{KNO3} to make 0.300 L of solution.

M=0.750.300=2.5 M M = \frac{0.75}{0.300} = 2.5 \text{ M}

If you were given 25.0 g instead, you would first convert grams → moles using molar mass.

Common mistakes I see:

  • Forgetting to convert mL to L
  • Plugging grams directly into the formula
  • Using solvent volume instead of total solution volume

On free response, unit consistency is often where points are lost.

Dilution and the M1V1=M2V2M_{1}V_{1} = M_{2}V_{2} Relationship

Dilution lowers concentration by adding solvent.

The critical idea is this: moles of solute stay constant.

Since M=nVM = \frac{n}{V}, then n=MVn = MV.
If no solute is added or removed:

M1V1=M2V2 M_{1}V_{1} = M_{2}V_{2}

  • M1,V1M_{1}, V_{1} → initial
  • M2,V2M_{2}, V_{2} → final

All volumes must use the same units.

Example

You have 0.800 M HCl\ce{HCl}. You take 50.0 mL and dilute it to 200.0 mL. What is the new molarity?

(0.800)(50.0)=M2(200.0) (0.800)(50.0) = M_{2}(200.0)

M2=0.200 M M_{2} = 0.200 \text{ M}

Notice how concentration dropped because volume increased.

On tests, they love wording like “solution was diluted to a final volume of…” That phrase tells you which value is V2V_{2}.

Key Takeaways

A solution is homogeneous, meaning macroscopic properties are the same throughout the sample.
“Aqueous” means dissolved in water, not just mixed with water.
Solutions can be solid, liquid, or gas as long as composition is uniform.
Molarity uses moles of solute divided by liters of solution, not solvent.
Always convert mL to L before using M=nVM = \frac{n}{V}.
Dilution works because the moles of solute stay constant, so M1V1=M2V2M_{1}V_{1} = M_{2}V_{2}.
In explanation questions, describe dissolving in terms of breaking and forming intermolecular forces.

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