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Energetics I

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

Standard Conditions - temp pressure and conc

Back (Answer)

Temp: 25 degrees celsius / 298K Pressure: 1 bar / 10^5 Pa Conc of aq solute: 1mol/dm^3

#2
Front (Question)

Defn of enthalpy and symbol High enthalpy = less/more stable?

Back (Answer)

Enthalpy (H) is a measure of energy content of a sub, hence reflecting its stability High enthalpy = less stable

#3
Front (Question)

Eqn for enthalpy

Back (Answer)

ΔHr = Σ (H prod / final) - Σ (H reactants / initial)

#4
Front (Question)

ΔH > 0 • meaning • energy profile diagram • energy lvl diagram • prod or reactants are more stable?

Back (Answer)

Endothermic - energy absorbed from surroundings & temp of surrounding decrease H prod > H rcts Products are less stable than rcts

#5
Front (Question)

ΔH < 0 • meaning • energy profile diagram • energy lvl diagram • prod or reactants are more stable?

Back (Answer)

Exothermic - energy released to surroundings & temp of surrounding increases H prod < H rcts Products are more stable than rcts

#6
Front (Question)

Defn of activation energy & symbol

Back (Answer)

Activation energy (Ea) is the min. energy the rct molecules must possess in order to collide successfully to form prod. It affects the speed of the rctn

#7
Front (Question)

Standard enthalpy change of rctn & symbol

Back (Answer)

ΔHrΘ The energy change when molar quantities of rcts specified in the chemical eqn reacts to form prod at 1 bar & 298K

#8
Front (Question)

All chem eqn must have …

Back (Answer)

State symbols

#9
Front (Question)

Measurement of Standard enthalpy change of rctn depends on (2)

Back (Answer)

• Amt of rcts and prod - if they are X2, then ΔH X2 - order is reversed then sign is opp • Phy state of the sub - Prod (l) is more stable than prod (g) so lower - Diamond is also more stable than graphite so lower

#10
Front (Question)

Defn of Hess’ Law

Back (Answer)

The enthalpy change accompanying a chem rctn is the same regardless of the route by which the chem change occurs, provided the initial and final conditions are the same.

#11
Front (Question)

5 steps of Hess’ Law

Back (Answer)

• Write balanced eqn • start energy cycle with most complicated eqn • complete cycle by adding in eqns…. • Write the corresponding ΔH values next to the arrows • Sum of CW arrows = sum of ACW arrows

#12
Front (Question)

Defn of standard enthalpy change of formation symbol eqn Common elements* For an element at std state … Stability of a sub relative to the constituent elements

Back (Answer)

ΔHfΘ is the enthalpy change when 1 mole of a species is formed from its constituent elements in their std states at 298K and 1 bar ΔHrΘ = Σ HfΘ (prod) - Σ HfΘ (reactants) FLAPPER Common elements: P4 (s), Br2 (l), S8 (s) For an element at std state, ΔHfΘ = 0 If ΔHfΘ < 0, then sub is more stable than the elements & vice versa

#13
Front (Question)

Defn of standard enthalpy change of combustion symbol eqn For org compounds with only C / H / O, prod are always…

Back (Answer)

ΔHcΘ is the heat evolved when 1 mole of a sub is completely burned in excess oxygen under std conditions of 298K and 1 bar ΔHrΘ = Σ HcΘ (rcts) - Σ HcΘ (prod) CRAP Prod are always CO2 (g) + H2O (l) Always exo

#14
Front (Question)

Defn of bond energies symbol eqn

Back (Answer)

Bond energies is the ave energy absorbed when breaking 1 mole of covalent bond in the gaseous state ΔHrΘ = Σ BE (rcts / bond broken) - Σ BE (prod / bonds formed) BURP

#15
Front (Question)

Requirement to use bond energies in calc

Back (Answer)

Rctn must take place in the gaseous state

#16
Front (Question)

Why might there be discrepancies in BE in DB

Back (Answer)

BE in DB are averaged across a large sample of molecules containing the covalent bond

#17
Front (Question)

Qn eg: Using relevant BE values in DB calc… state and explain if the and in (a) is an estimate/exact value

Back (Answer)

Exact value as the BE used in calc are exact values obtained from the DB as HCL is a heteronuclear molecules, while H2 and CO2 are homonuclear molecules and all in gaseous state

#18
Front (Question)

Defn of bond dissociation energy of a X-Y bond

Back (Answer)

Energy required to break 1 mole of that particular X-Y bond in a particular compound in gaseous state

#19
Front (Question)

Defn of standard enthalpy change of hydration symbol Mag depends on eqn eg

Back (Answer)

ΔHhydΘ is the energy released when 1 mole of a gaseous ion is dissolved in a large amt of water at 298K and 1 bar |ΔHhydΘ| ∝ |charge of ion/size of ion| (charge density) Na+ (g) -> Na+ (aq)

#20
Front (Question)

Why is std enthalpy change of hydration is exo

Back (Answer)

Energy is released during the formation of ion-dipole interactions Larger charge density - more exo ΔHhydΘ - stronger ion-dipole interactions

#21
Front (Question)

Defn of std enthalpy change of soln symbol soluble/insoluble

Back (Answer)

ΔHsolΘ is the enthalpy change when 1 mole of solute is completely dissolved in a solvent to form an infinitely dilute soln under std conditions of 298K and 1 bar (usually a solid ionic compound) ΔHsolΘ»_space; insoluble in water ΔHsolΘ < soluble in water

#22
Front (Question)

Defn of lattice energy Symbol Mag depends on

Back (Answer)

ΔHlattΘ is the heat evolved when 1 mole of a solid ionic compound is formed from its constituent gaseous ions under std conditions of 298K and 1 bar |ΔHlattΘ| ∝ | q+ x q- / r+ + r- |

#23
Front (Question)

Eqn for ΔHsolΘ

Back (Answer)

ΔHsolΘ = Σ ΔHhydΘ - Σ ΔHlattΘ fav soln is hyd latte

#24
Front (Question)

Is Lattice energy exo/endo and why

Back (Answer)

Exo as Energy is released when strong electrostatic forces of attraction are formed b/w cations and anions