Intuition What this page is for
The parent note built the formula. Here we stress-test it against every situation a problem can throw at you : normal numbers, the degenerate edges (v = 0 , T → 0 , T → ∞ ), limiting behaviour, a real propulsion word-problem, and an exam-style twist. If you can do all of these, no MB question will surprise you.
Everything below uses only two constants and one formula, so let us pin them once.
Definition The toolkit (nothing new after this line)
k B = 1.38 × 1 0 − 23 J/K — Boltzmann's constant, the bridge from temperature to energy.
m — mass of one molecule (kilograms), not the molar mass.
The speed distribution:
f ( v ) = 4 π ( 2 π k B T m ) 3/2 v 2 e − 2 k B T m v 2
The three speeds, all sharing the factor k B T / m :
v p = m 2 k B T , v ˉ = π m 8 k B T , v r m s = m 3 k B T .
Every MB problem is one (or a blend) of these case classes . The last column says which worked example covers it.
#
Case class
What makes it tricky
Covered by
C1
Plain numeric speed
Get m from molar mass right
Ex 1
C2
Ratio / universal
k B T / m cancels — answer is pure number
Ex 2
C3
Temperature scaling
All speeds ∝ T
Ex 3
C4
Mass scaling (propulsion)
All speeds ∝ 1/ m
Ex 4
C5
Degenerate input v = 0
f ( 0 ) = 0 , not a peak
Ex 5
C6
Limiting T → 0 and T → ∞
Curve collapses / spreads
Ex 5
C7
Peak height vs peak position
Height falls as T rises
Ex 6
C8
Fraction in a speed window (integral)
Needs the f ( v ) d v meaning
Ex 7
C9
Real-world word problem (nozzle)
Turn physics into v r m s
Ex 8
C10
Exam twist: mixture / two gases
Each gas keeps its own m
Ex 9
Worked example RMS and mean speed of oxygen O₂ at 300 K
Molar mass of O₂ is M = 32 g/mol = 0.032 kg/mol . Avogadro N A = 6.022 × 1 0 23 . Find v r m s and v ˉ at T = 300 K .
Forecast: N₂ was ≈ 517 m/s in the parent. O₂ is slightly heavier (32 vs 28). Guess: a bit below 500 m/s.
Step 1 — Get the mass of one molecule.
m = N A M = 6.022 × 1 0 23 0.032 = 5.31 × 1 0 − 26 kg .
Why this step? The formula needs mass per molecule, not per mole — this is the #1 place people slip.
Step 2 — Plug into v r m s = 3 k B T / m .
v r m s = 5.31 × 1 0 − 26 3 ( 1.38 × 1 0 − 23 ) ( 300 ) = 2.339 × 1 0 5 ≈ 484 m/s .
Why this step? "rms" weights the fast molecules — the speed relevant to pressure and energy.
Step 3 — Mean speed via the fixed ratio v ˉ / v r m s = 8/ π / 3 = 8/ ( 3 π ) .
v ˉ = v r m s 3 π 8 = 484 × 0.9213 ≈ 446 m/s .
Why this step? Once you have one speed, the others are just constant multiples — no need to re-integrate.
Verify: 484 m/s is just under 500 and below N₂'s 517 (O₂ heavier ⟹ slower) ✓. Units: J / kg = m 2 / s 2 = m/s ✓.
v p / v r m s for any gas
Show that the ratio of most-probable to rms speed is a pure number, and evaluate it.
Forecast: v p sits at the peak, v r m s is pulled right by the tail. So the ratio should be less than 1 — guess around 0.8.
Step 1 — Write both.
v r m s v p = 3 k B T / m 2 k B T / m .
Why this step? Both carry the identical factor k B T / m — writing them side by side exposes the cancellation.
Step 2 — Cancel k B T / m .
v r m s v p = 3 2 = 0.8165.
Why this step? Because the physics (k B , T , m ) drops out, this number is the same for every gas at every temperature — a signature of the shape of the curve.
Verify: 0.8165 < 1 ✓ (peak is left of rms). Cross-check via the parent's ratio 1.000 : 1.128 : 1.225 : 1/1.225 = 0.816 ✓.
Worked example Heating from 300 K to 1200 K
A gas is heated so T goes from 300 K to 1200 K . By what factor does v r m s change?
Forecast: T went up × 4 . Speed depends on T , so guess × 2 .
Step 1 — Use v r m s ∝ T (mass cancels since same gas).
v r m s ( 300 ) v r m s ( 1200 ) = 300 1200 = 4 = 2.
Why this step? When only T changes, everything else is a constant multiplier that cancels in a ratio — no need for actual numbers.
Verify: 4 × the temperature ⟹ 2 × the speed ⟹ 4 × the kinetic energy (E ∝ v 2 ∝ T ) — consistent with "energy is linear in T " ✓.
Worked example Helium vs xenon as thruster propellant
Compare v r m s of He (M = 4 g/mol ) and Xe (M = 131 g/mol ) at the same temperature. Which makes a better cold-gas thruster (higher exhaust speed = more specific impulse )?
Forecast: Xe is ≈ 33 × heavier. Speed ∝ 1/ m , so He should be roughly 33 ≈ 5.7 × faster.
Step 1 — Same T , so v r m s ∝ 1/ m , and molar mass ratio equals molecular mass ratio.
v Xe v He = M He M Xe = 4 131 = 32.75 .
Why this step? The heavier mass sits under a square root in the denominator, so it enters as 1/ m ; the ratio wipes out k B T .
Step 2 — Evaluate.
v Xe v He = 5.72.
Why this step? This is the whole reason light gases give more thrust per kilogram — the exhaust leaves far faster.
Verify: He faster than Xe ✓, and magnitude near the forecast 5.7 ✓. (Consistent with Graham's law , rate ∝ 1/ m .)
Worked example What happens at
v = 0 , and as T → 0 or T → ∞ ?
Evaluate f ( 0 ) , and describe the curve in the two temperature limits.
Forecast: At v = 0 nothing is moving — should be rare , so f ( 0 ) small. At T → 0 everything freezes; at T → ∞ everything spreads out.
Step 1 — Plug v = 0 into the formula.
f ( 0 ) = 4 π ( 2 π k B T m ) 3/2 ⋅ 0 2 ⋅ e 0 = 0.
Why this step? The v 2 shell factor kills the value: there is zero surface area on a sphere of radius 0 , so no velocity vectors have exactly zero speed. The curve starts at the origin, not at a peak.
Step 2 — Limit T → 0 . Then v p = 2 k B T / m → 0 and the Gaussian width shrinks — the whole curve collapses into a spike at v = 0 .
Why this step? No thermal energy means no motion; a distribution of a single value 0 is a spike.
Step 3 — Limit T → ∞ . Then v p → ∞ , the peak marches right, the curve flattens and widens (area stays 1 ).
Why this step? Infinite heat spreads molecules over all speeds; probability must stay normalized, so height drops as width grows.
Verify (figure): the three curves below show exactly this — cold = tall narrow spike near zero, hot = short wide curve far right, and all three touch 0 at v = 0 ✓.
Worked example Does a hotter gas have a taller peak?
As T increases, does the height of f ( v ) at its peak go up or down? Find how the peak height scales with T .
Forecast: The peak moves right (faster). Since total area is fixed at 1 , a curve that spreads wider must get shorter . Guess: height falls.
Step 1 — The peak sits at v p = 2 k B T / m . Substitute v = v p into f ( v ) . Note m v p 2 / ( 2 k B T ) = 1 , so the exponential becomes e − 1 .
f ( v p ) = 4 π ( 2 π k B T m ) 3/2 v p 2 e − 1 .
Why this step? Evaluating at the peak turns the messy exponent into the constant e − 1 , isolating the T -dependence.
Step 2 — Track the powers of T . The prefactor gives T − 3/2 ; v p 2 = 2 k B T / m gives T + 1 .
f ( v p ) ∝ T − 3/2 ⋅ T + 1 = T − 1/2 .
Why this step? Collecting all T 's tells us the height scales as 1/ T — it falls as the gas heats.
Verify: From 300 K to 1200 K (× 4 ), peak height → ( 4 ) − 1/2 = 1/2 of its value. In the figure from Ex 5 the hottest curve is indeed the shortest ✓. Area under each curve stays 1 (spread up, height down) ✓.
Worked example Fraction with speed within
± 1% of v p
Estimate the fraction of molecules with speed between v p and 1.01 v p (a thin window right at the peak) using f ( v ) d v .
Forecast: A 1% window is thin. Roughly (fraction) ≈ f ( v p ) × (window width). Guess: about 1%.
Step 1 — Use the definition: fraction ≈ f ( v p ) Δ v with Δ v = 0.01 v p .
Why this step? f ( v ) d v is the fraction in a narrow slice; near the peak f is almost flat, so a rectangle is a good approximation.
Step 2 — Compute f ( v p ) in units of v p . With β = 1/ v p 2 the formula gives
f ( v p ) = π 4 v p 1 e − 1 = π 4 e − 1 v p 1 = 0.8302 v p 1 .
Why this step? Writing everything in terms of v p makes the v p 's cancel with Δ v , leaving a pure number.
Step 3 — Multiply by the window.
fraction ≈ 0.8302 v p 1 × 0.01 v p = 8.30 × 1 0 − 3 ≈ 0.83%.
Why this step? This is the concrete meaning of "fraction of molecules" — an actual small number you could count.
Verify: Result is dimensionless ✓ (units of v p cancelled), positive, and less than 1% as forecast ✓.
Worked example Exhaust speed of a hot-hydrogen thruster
A nuclear-thermal rocket heats hydrogen gas (H₂, M = 2 g/mol ) to 2800 K before it leaves the nozzle. Estimate the characteristic thermal speed v r m s of the H₂ molecules. Why does this hint at a high specific impulse?
Forecast: Very light gas, very hot — expect several thousand m/s.
Step 1 — Mass of one H₂ molecule.
m = 6.022 × 1 0 23 0.002 = 3.32 × 1 0 − 27 kg .
Why this step? Again convert molar → per-molecule before touching k B .
Step 2 — Compute v r m s = 3 k B T / m .
v r m s = 3.32 × 1 0 − 27 3 ( 1.38 × 1 0 − 23 ) ( 2800 ) = 3.491 × 1 0 7 ≈ 5908 m/s .
Why this step? v r m s sets the energy scale of the exhaust; nearly 6 km/s is the thermal speed feeding the directed jet.
Step 3 — Interpret. Specific impulse ∝ exhaust velocity ∝ v r m s ∝ 1/ m . Hydrogen's tiny m is what makes its molecules so fast at a given T .
Why this step? Ties the number back to the propulsion payoff from the parent note.
Verify: ∼ 5900 m/s is in the expected thousands ✓. Compare to O₂ at 300 K (484 m/s): H₂ is lighter (× 16 ) and hotter (× 9.3 ), factor 16 × 9.3 = 12.2 , and 484 × 12.2 = 5905 ✓.
Worked example Same box, two gases — do they share a speed?
A sealed box holds He and Ar in thermal equilibrium at one temperature T . A student claims "in equilibrium both gases have the same v r m s ." True or false? Find the ratio v r m s , He / v r m s , Ar (M He = 4 , M Ar = 40 g/mol).
Forecast: Equilibrium means equal temperature (equal mean energy), not equal speed. Lighter He must move faster. Guess ratio ≈ 10 ≈ 3.2 .
Step 1 — Equilibrium equalises average kinetic energy per molecule (via equipartition ): 2 1 m ⟨ v 2 ⟩ = 2 3 k B T for each gas.
Why this step? Temperature — not speed — is what two gases share when they mix. The student confused "same T " with "same v ."
Step 2 — Equal energy but different mass ⟹ different speed. Take the ratio.
v r m s , Ar v r m s , He = M He M Ar = 4 40 = 10 = 3.162.
Why this step? With k B T fixed (same box), only mass differs, entering as 1/ m .
Step 3 — Verdict: the claim is false ; only v r m s , He = 10 v r m s , Ar holds.
Why this step? Names the specific misconception so it never recurs.
Verify: He faster ✓, ratio 3.16 > 1 ✓; equal energies check: 2 1 m He v He 2 vs 2 1 m Ar v Ar 2 have ratio ( 1/10 ) ( 10 ) = 1 ✓.
Recall Which cell was hardest? Self-test
Peak height of f ( v ) scales as ::: T − 1/2 (falls as gas heats).
f ( 0 ) = ? and why ::: 0 , because the v 2 shell factor vanishes at zero speed.
Two gases mixed at equilibrium share ::: temperature (mean energy), not speed.
v p / v r m s for any gas ::: 2/3 = 0.8165 , universal.