Thermochemistry

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29 Terms

1
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What is energy?

Energy is just the ability to do something:

  • move

  • make heat

  • make things happen

Example:

  • Food gives you energy to walk

  • Gas gives a car energy to move

  • Fire gives energy as heat

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Law of Conservation of Energy

Big rule:
Energy cannot be created
Energy cannot be destroyed
Energy can only change form

Example:

  • Gas → heat → movement

  • Food → body heat + motion

👉 The total energy in the universe stays the same.

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Ways Energy Moves (Transfers)

🔥 “Heat = energy moving because of temperature difference”

This just means:

👉 Heat is energy that moves ONLY because one thing is hotter than another.

If two things are the same temperature, NO heat moves.


🌡 “Hot → cold (ALWAYS)”

This means:

👉 Heat always moves from the hot thing to the cold thing.

Examples:

  • Hot coffee sitting on a table → coffee cools down, table/air warms up

  • Hot shower → bathroom warms up

  • Your hand on ice → your hand loses heat, ice gains heat

This happens automatically. No effort needed.


“Never cold → hot by itself”

This means:

👉 Cold things cannot heat up hotter things on their own.

Example:

  • Ice will NEVER make your hand hotter

  • A cold room will not heat your body

For cold → hot to happen, you need extra energy (like a heater, stove, microwave).


🏃 “Temperature tells us how fast particles are moving”

This is the KEY idea 👶:

  • Hot = particles moving fast

  • Cold = particles moving slow

So:

  • Hot coffee → molecules zooming around

  • Cold water → molecules moving slowly

When hot touches cold:
👉 fast particles bump into slow ones
👉 fast ones slow down
👉 slow ones speed up
👉 eventually they’re the same speed (same temperature)


🧠 ONE-LINE MEMORY TRICK (EXAM GOLD)

  • Heat = energy in motion

  • Temperature = how fast particles move

  • Heat flows hot → cold, NEVER the other way

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🏋 Work

Work = force moving something

  • Pushing a box

  • Expanding a gas

  • Lifting a weight

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Pathway

🛣 “Pathway = HOW energy moves”

Pathway just means:
👉 the route or method energy takes to move

Not where it starts or endsHOW it gets there


“Total energy change does NOT depend on the path”

This means:

👉 Only the starting point and ending point matter
👉 It does NOT matter how you got there

Real-life example (this is the key):

You start:

  • At the bottom of a hill

You end:

  • At the top of the hill

No matter what:

  • You climbed

  • You drove

  • You zig-zagged

👉 You end at the same height
👉 Same total energy change


🔥 “Heat and work DO depend on the path”

This is the part that trips people.

It means:

👉 How tired you get depends on HOW you go up
👉 How much heat or work happens depends on the path

Same hill example:

🚶‍♂ Walk up:

  • You sweat a lot (more heat)

  • You use more effort (more work)

🚗 Drive up:

  • Less effort from YOU

  • Engine does the work instead

Same start
Same end
Different heat & work


🧠 Chem Translation (VERY IMPORTANT)

In chemistry:

  • Total energy change (ΔE) → does NOT care about path

  • Heat (q) and Work (w) → CARE about path

That’s why:

ΔE=q+w

Different paths → different q and w
But same ΔE


🧠 ONE-LINE BABY SUMMARY (EXAM SAFE)

  • Start + End decide total energy

  • Path decides heat & work

  • Same place → same ΔE

  • Different routes → different q and w


🚨 EXAM TRAP TO WATCH FOR

If they ask:

“Does energy change depend on pathway?”

Answer:
NO (for total energy)

If they ask:

“Does heat depend on pathway?”

Answer:
YES

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State Function

OFFICIAL DEFINITION (EXAM-SAFE)

A state function is a property whose value depends only on the current state of the system and not on the path taken to reach that state.

👉 That sentence is what you memorize.


🧠 NOW TRANSLATED INTO NORMAL ENGLISH

  • Property = something you can measure (energy, temperature, etc.)

  • Current state = what the system looks like right now

  • Not on the path = doesn’t care how it happened

So in human words:

A state function only depends on where the system starts and ends, not how it got there.


🧪 CHEM EXAMPLE

If a reaction starts with:

  • 100 J of energy

and ends with:

  • 50 J of energy

Then:

  • ΔE = −50 J

No matter:

  • fast reaction

  • slow reaction

  • one step

  • many steps

👉 SAME ΔE every time


🧠 ONE-LINE EXAM MEMORY

State function = depends only on initial and final state


🚨 VERY COMMON EXAM QUESTION

Which is a state function?

Energy
Enthalpy
Temperature

Heat
Work

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Heat Flow

Heat ALWAYS flows:
👉 Hot → Cold

Why?

  • Hot particles move faster

  • Cold particles move slower

  • They share energy until equal

When equal → same temperature

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System vs Surroundings

🧪 System

The thing you care about

  • The reaction

  • Chemicals reacting

🌍 Surroundings

Everything else

  • Air

  • Table

  • Room

  • You

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Types of Reactions

🔥 Exothermic

  • Heat leaves the system

  • System gets colder

  • Surroundings get warmer

Example:

  • Fire

  • Hand warmers

  • Combustion

ΔH is negative (−)

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Endothermic

  • Heat enters the system

  • System gets warmer

  • Surroundings get colder

Example:

  • Ice melting

  • Cold packs

ΔH is positive (+)

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Thermodynamics

Thermodynamics = study of energy and how it changes

First Law:
👉 Energy is conserved (same rule again)

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Internal Energy (E)

🧠 WHAT “INTERNAL ENERGY (E)” ACTUALLY MEANS Internal energy = ALL the energy INSIDE the system

That’s it.

If the system is:

  • a beaker

  • a reaction

  • a gas in a container

👉 Internal energy is the energy stored in that thing


🔹 WHAT MAKES UP INTERNAL ENERGY? 1⃣ Particle motion

This is just:

  • particles moving

  • vibrating

  • zooming around

👉 This is kinetic energy

Hotter = faster particles
Colder = slower particles


2⃣ Attractions between particles

This is:

  • particles pulling on each other

  • bonds

  • intermolecular forces

👉 This is potential energy

Strong attractions = more stored energy


🔹 HOW CAN INTERNAL ENERGY CHANGE?

Only two ways:

🔥 Heat (q)

  • Energy moves because of temperature difference

  • Hot cold

If heat enters system:

  • q is positive

  • internal energy increases

If heat leaves system:

  • q is negative

  • internal energy decreases


🏋 Work (w)

  • Energy moves because something is pushed, pulled, or expanded

Example:

  • Gas expands → does work → loses energy

  • Gas is compressed → gains energy


🔹 THE MONEY FORMULA 💰 ΔE=q+w

Translation:

Change in internal energy = heat + work


🧠 ONE-LINE BABY SUMMARY

  • Internal energy = energy stored inside

  • Comes from particle motion + attractions

  • Can ONLY change by:

    • heat

    • work


🚨 EXAM TRAP TO WATCH

They might ask:

“Which can change internal energy?”

Answer:
Heat
Work

NOT:
temperature by itself
mass
pathway


🧠 CAVEMAN MODE 🦴

System has energy
Heat in → energy up
Work out → energy down

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ΔE Equation

ΔE=q+w

  • q = heat

  • w = work

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Signs (+ / −) — VERY IMPORTANT

From the SYSTEM’S view:

q positive (+)
→ heat enters system (endothermic)

q negative (−)
→ heat leaves system (exothermic)

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Enthalpy (H)


🧠 WTF IS ENTHALPY (H) — BABY MODE Enthalpy is just a special way of talking about energy

👉 when pressure stays constant (which is almost always in lab).

That’s it.


🔹 “Energy at constant pressure” — WHAT THAT MEANS

In most chemistry labs:

  • reactions happen in open containers

  • pressure = atmospheric pressure

  • pressure does NOT change

So chemists said:

“Let’s define a type of energy that works nicely when pressure is constant.”

That energy is called enthalpy (H).


🔹 WHY DO WE CARE ABOUT ENTHALPY?

Because in constant-pressure conditions:

ΔH=heat gained or lost\Delta H = \text{heat gained or lost}ΔH=heat gained or lost

Meaning:
👉 ΔH tells you how much heat the reaction releases or absorbs


🔹 WHY YOU DON’T MEASURE H DIRECTLY

Because:

  • H is like a bank balance from birth

  • You don’t know the starting value

But you CAN measure:
👉 how much it changes

That’s ΔH.

Same as:

  • You don’t know how much money you had at age 3

  • But you know how much you spent today


🔹 WHAT ΔH TELLS YOU 🔥 Exothermic

  • Heat leaves system

  • ΔH negative

  • Products have LESS energy

Endothermic

  • Heat enters system

  • ΔH positive

  • Products have MORE energy


🧠 ONE-LINE EXAM DEFINITION

Enthalpy is a state function that represents the heat content of a system at constant pressure.

Memorize that 👆


🧠 CAVEMAN MODE 🦍

Pressure same
Reaction happens
Heat measured = ΔH


🚨 EXAM TRAP

If they ask:

“When is ΔH equal to heat?”

Answer:
At constant pressur

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ΔH at Constant Pressure

At constant pressure:

ΔH= q ^p

Meaning:
👉 Heat measured = enthalpy change

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Comparing Enthalpy

  • Products HIGHER → ΔH positive → endothermic

  • Products LOWER → ΔH negative → exothermic

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Calorimetry

🧠 WTF IS CALORIMETRY (BABY MODE) Calorimetry = measuring heat

That’s it.
Nothing mystical.

You can’t see heat directly, so instead you:

👉 watch temperature change


🔥 WHY TEMPERATURE?

Because:

  • Heat going in → temperature goes up

  • Heat going out → temperature goes down

So temperature is like a thermometer spy telling you about heat.


REAL EXAMPLE (COFFEE CUP)

  • You mix two chemicals in a cup

  • Reaction happens

  • Thermometer moves

If temp:

  • goes UP → reaction released heat (exothermic)

  • goes DOWN → reaction absorbed heat (endothermic)


🧠 CHEM TRANSLATION

Calorimetry works because:

q=mcΔTq = m c \Delta Tq=mcΔT

You don’t need to panic — this just means:

  • mass

  • heat capacity

  • temperature change

tell you how much heat moved.


🧠 ONE-LINE EXAM DEFINITION (MEMORIZE)

Calorimetry is the experimental measurement of heat associated with a physical or chemical process by observing temperature change.


🚨 EXAM TRAP

If they ask:

“How is heat measured in calorimetry?”

Answer:
By measuring temperature change

NOT:
directly weighing heat
measuring pressure
watching color change


🧠 CAVEMAN MODE 🦴

Reaction happens
Temperature moves
Heat happened

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Heat Capacity (C)

Heat capacity = how hard it is to heat something up

Specific heat

  • Per gram

Molar heat

  • Per mole

Water has HIGH heat capacity
→ heats slowly
→ cools slowly

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Coffee Cup Calorimeter

  • Styrofoam cups

  • Measures heat at constant pressure

  • Used for reactions in solution

If temperature:

  • Goes UP → exothermic

  • Goes DOWN → endothermic

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Heat Is Extensive

More substance = more heat

Double reaction → double heat

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Bomb Calorimeter 💣

ONE-SENTENCE MEMORY (THIS IS THE GOAL)

In a bomb calorimeter, the container cannot expand, so no work is done and all the energy change appears as heat.


CAVEMAN MODE 🦴

Box locked
Fire inside
No pushing
Only heat

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Mixing Temperatures

🧠 WHAT “MIXING TEMPERATURES” MEANS

You mix:

  • one hot thing

  • one cold thing

Heat flows:
👉 hot → cold

They keep exchanging heat until:
👉 same temperature

That temperature is the final temperature.


🔹 WHY FINAL TEMP IS BETWEEN THE TWO

Example:

  • Hot water: 80°C

  • Cold water: 20°C

Final temperature:
👉 cannot be 100°C (no extra heat)
👉 cannot be 0°C (no freezer)

So it must be:
👉 between 20°C and 80°C

This is ALWAYS true.


🔹 WHY SOMETIMES IT’S NOT THE MIDDLE

Now the important part 👇

Heat capacity matters

If one thing:

  • has higher heat capacity

  • or more mass

it controls the final temperature more.


🔥 EASY EXAMPLE Case 1: Same stuff, same amount

  • 50 g hot water at 80°C

  • 50 g cold water at 20°C

Final temp:
👉 around 50°C


Case 2: Different heat capacity

  • 50 g water at 20°C

  • 50 g iron at 80°C

Water has higher heat capacity than iron.

So:

  • water changes temp less

  • final temp is closer to water’s temp

👉 NOT 50°C


🧠 ONE-LINE RULE (EXAM GOLD)

The final temperature lies between the initial temperatures and is closer to the substance with the higher heat capacity.


🧠 CAVEMAN MODE 🦴

Hot gives heat
Cold takes heat
Meet in middle

Big heat sponge decides where


🚨 EXAM TRAP

If they ask:

“Which ends up with the smaller temperature change?”

Answer:
the substance with higher heat capacity

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Hess’s Law

Doesn’t matter HOW reaction happens
Only START and END matter

Steps don’t change ΔH

Rules for ΔH

  • Reverse reaction → flip sign

  • Multiply equation → multiply ΔH

  • Scale reaction → scale ΔH

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Standard Enthalpy of Formation (ΔH°f)

👉 1 mole of compound forms
👉 from elements in standard states

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Standard States

  • Gas → 1 atm

  • Solid/Liquid → pure

  • Solution → 1 M

  • Elements → natural form

Example:

  • O₂ (g)

  • Na (s)

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Important Rule

Elements in standard state:

ΔH^f= 0

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Enthalpy Calculations Formula

ΔHrxn​=∑(ΔHf∘​ products)−∑(ΔHf∘​ reactants)

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EXAM SURVIVAL SUMMARY

  • Exothermic → ΔH negative

  • Endothermic → ΔH positive

  • Heat flows hot → cold

  • System POV matters

  • Elements in standard state = 0

  • Hess’s Law = steps don’t matter