This page is the exhaustive drill sheet for the Maxwell-Boltzmann distribution . The parent note derived the curve; here we hit every kind of question it can throw at you — every limiting case, every degenerate input, every sign, plus a word problem and an exam twist.
Before we start, one reminder of the two objects we will use over and over.
Definition The two distributions (say them out loud)
Single-component distribution — for ONE axis of velocity, e.g. v x :
g ( v x ) = ( 2 π k B T m ) 1/2 e − m v x 2 /2 k B T .
This is a symmetric bell (Gaussian) centred at zero : v x can be negative (moving left) or positive (moving right). It is normalized over the whole line: ∫ − ∞ ∞ g ( v x ) d v x = 1 .
Speed distribution — for the magnitude v = v x 2 + v y 2 + v z 2 ≥ 0 :
f ( v ) = 4 π ( 2 π k B T m ) 3/2 v 2 e − m v 2 /2 k B T .
This starts at f ( 0 ) = 0 , rises, peaks, falls. Speed is never negative , so this curve lives only on the right half, and it is normalized there: ∫ 0 ∞ f ( v ) d v = 1 .
Here m = mass of one molecule (kg), k B = 1.38 × 1 0 − 23 J/K (Boltzmann's constant, the "energy per kelvin per molecule"), T = temperature (K). The symbol N₂ below just means a nitrogen molecule (two nitrogen atoms bonded, molar mass 28 g/mol); O₂ is an oxygen molecule (32 g/mol). The three landmark speeds are
v p = m 2 k B T , ⟨ v ⟩ = π m 8 k B T , v r m s = m 3 k B T .
Every question about this distribution falls into exactly one of these case classes . The examples below are labelled by which cell they fill.
Cell
Case class
What is "extreme" about it
Example
A
Plug-and-chug landmark speed
ordinary numbers
Ex 1
B
Sign / direction of a component
v x < 0 vs v x > 0 , both halves
Ex 2
C
Degenerate input v = 0
speed exactly zero
Ex 3
D
Limiting behaviour v → ∞
the far tail
Ex 4
E
Limit T → 0 and T → ∞
freezing / infinitely hot
Ex 5
F
Heavy vs light molecule at same T
mass extremes
Ex 6
G
Real-world word problem
escape from atmosphere
Ex 7
H
Exam twist — dimensionless ratio
temperature/mass cancel
Ex 8
I
Fraction in a finite band
an integral you must set up
Ex 9
We now walk cells A→I.
Worked example Mean speed of oxygen (O₂) at
T = 300 K
One O₂ molecule has mass m = 32 × 1.66 × 1 0 − 27 = 5.31 × 1 0 − 26 kg .
Find the mean speed ⟨ v ⟩ .
Forecast: A nitrogen molecule (N₂, molar mass 28 g/mol) at 300 K has a most-probable speed near 420 m/s. O₂ is heavier than N₂, so guess a bit slower — a few hundred m/s. Write your guess down.
Step 1. Pick the right formula. We want the mean , so use ⟨ v ⟩ = 8 k B T / ( π m ) .
Why this step? Three landmark speeds exist; "mean" specifically carries the factor 8/ π , not 2 or 3.
Step 2. Assemble the numerator inside the root: 8 k B T = 8 ( 1.38 × 1 0 − 23 ) ( 300 ) = 3.312 × 1 0 − 20 .
Why this step? Group all constants before dividing, so units stay clean (J = kg·m²/s²).
Step 3. Divide and take the root:
⟨ v ⟩ = π ( 5.31 × 1 0 − 26 ) 3.312 × 1 0 − 20 = 1.986 × 1 0 5 ≈ 446 m/s .
Why this step? The root converts (m²/s²) back to (m/s).
Verify: Units: J / kg = m 2 / s 2 = m/s ✓. Value ~446 m/s, in the "few hundred" range we forecast ✓.
Worked example Fraction of molecules moving
leftward faster than v p along x
Using the single-component Gaussian g ( v x ) , what fraction have v x < − v p ? (Here − v p means moving in the − x direction with a component speed exceeding the most-probable speed magnitude.)
Forecast: g is symmetric about 0, so leftward and rightward tails are equal. Guess: "same as the fraction with v x > + v p ."
Step 1. Recognise symmetry: g ( − v x ) = g ( v x ) because it depends only on v x 2 .
Why this step? It converts the leftward question into an equivalent rightward one — no new integral.
P ( v x < − v p ) = P ( v x > + v p ) .
Step 2. Rescale by substituting u = v x / v p . Two things change together:
The exponent : since v p 2 = 2 k B T / m , we get 2 k B T m v x 2 = v p 2 v x 2 = u 2 .
The measure (Jacobian) : v x = u v p so d v x = v p d u — every slice of width d v x becomes a slice of width v p d u .
Now track the prefactor. Writing g ( v x ) d v x and substituting both pieces:
g ( v x ) d v x = ( 2 π k B T m ) 1/2 e − u 2 ( v p d u ) .
The prefactor times the Jacobian is ( 2 π k B T m ) 1/2 v p . Since v p = 2 k B T / m , that product is 2 π k B T m ⋅ m 2 k B T = π 1 = π 1 . So
P ( v x > v p ) = π 1 ∫ 1 ∞ e − u 2 d u = 2 1 erfc ( 1 ) .
Why this step? We must carry the Jacobian d v x = v p d u , otherwise the integral would be off by a factor v p . The Jacobian is exactly what cancels the dimensional part of the prefactor, leaving the clean dimensionless number 1/ π — the standard normalised Gaussian tail (which is the erfc integral defined above).
Step 3. Evaluate: erfc ( 1 ) = 0.1573 , so P = 2 1 ( 0.1573 ) = 0.0786 ≈ 7.9% .
Why this step? erfc ( z ) is our "area past z " function; here z = 1 because u = v p maps to 1.
Verify: In figure s01 the two red shaded tails (the leftward tail u < − 1 and the rightward tail u > 1 of the symmetric bell g ) are mirror images, each carrying ~7.9% of the area, with dashed vertical lines marking ± v p . Total in both tails = 15.7% , leaving 84% with ∣ v x ∣ < v p , which matches a Gaussian's "most of the mass near the centre" ✓.
Figure s01: The symmetric single-component Gaussian g ( v x ) plotted against v x / v p ; the two red-shaded regions beyond ± 1 are the equal tails, each ~7.9% of the total area.
f ( 0 ) , and how many molecules are exactly at rest?
Forecast: The Boltzmann factor e 0 = 1 is maximal at v = 0 . Naïve guess: "most molecules are near rest." Is that right?
Step 1. Plug v = 0 into f ( v ) = 4 π ( ⋯ ) v 2 e − ⋯ . The v 2 factor gives 0 .
Why this step? f is a product ; if any factor is 0 the whole thing is 0, no matter how large the exponential.
f ( 0 ) = 4 π ( ⋯ ) ⋅ 0 ⋅ 1 = 0.
Step 2. Interpret. "Exactly at rest" needs v x = v y = v z = 0 simultaneously — a single point in 3D velocity space, which has zero volume .
Why this step? The shell 4 π v 2 d v shrinks to nothing as its radius → 0 .
Verify: In figure s02 the red speed curve visibly touches zero at the origin then climbs to its hump. Compare with the dashed single-component Gaussian, which is maximal at 0. The difference is purely the geometric v 2 shell factor ✓.
Figure s02: Red = speed distribution f ( v ) , which starts at f ( 0 ) = 0 ; dashed black = a velocity-component Gaussian, which peaks at the origin. The gap between them is the v 2 shell factor.
f ( v ) ever stop decreasing, and how fast does the tail die?
Forecast: Guess whether the falling exponential eventually always wins over the rising v 2 .
Step 1. Compare the two factors for large v . v 2 grows polynomially ; e − α v 2 (with α = m /2 k B T > 0 ) decays super-exponentially .
Why this step? A key limit: lim v → ∞ v 2 e − α v 2 = 0 , because an exponential of v 2 beats any power of v .
Step 2. Find where the curve turns over, right here on this page. Set the derivative of v 2 e − α v 2 to zero:
d v d ( v 2 e − α v 2 ) = ( 2 v − 2 α v 3 ) e − α v 2 = 0 ⇒ 1 = α v 2 ⇒ v = α 1 = m 2 k B T = v p .
So the single peak sits at v p ; the curve rises for v < v p and falls monotonically for v > v p .
Why this step? This locates the one hump without borrowing from any other page — the tail we care about is everything to the right of v p .
Step 3. Estimate the tail at, say, v = 3 v p : exponent = α v 2 = α ( 9/ α ) = 9 , so factor e − 9 ≈ 1.23 × 1 0 − 4 . Relative to the peak, the height ratio f ( 3 v p ) / f ( v p ) = 9 e − 9 / ( 1 ⋅ e − 1 ) = 9 e − 8 ≈ 3.0 × 1 0 − 3 .
Why this step? Numbers make "the tail is tiny but nonzero" concrete — 0.3% of the peak height.
Verify: 9 e − 8 = 9 ( 3.355 × 1 0 − 4 ) = 3.02 × 1 0 − 3 ✓. The tail never reaches zero for finite v but is negligible — this is why some fast molecules can always escape (see Ex 7).
Worked example What shape does
f ( v ) approach as the gas freezes (T → 0 ) or becomes infinitely hot (T → ∞ )?
Forecast: Guess where the peak v p = 2 k B T / m goes in each limit.
Step 1 (T → 0 ). v p → 0 and the exponent − m v 2 /2 k B T → − ∞ for any v > 0 , so the curve is pushed to zero everywhere except right at the origin. But the height prefactor ( 2 π k B T m ) 3/2 → ∞ as T → 0 . These two effects are not in conflict — they cooperate:
the width of the surviving region shrinks like v p ∝ T → 0 ,
the prefactor blows up like T − 3/2 → ∞ ,
and they blow up/shrink at exactly the rate that keeps ∫ 0 ∞ f ( v ) d v = 1 at every temperature. The limiting object is therefore an infinitely tall, infinitely thin spike of unit area at v = 0 — a Dirac delta δ ( v ) (a "spike of area 1").
Why this step? Without the diverging prefactor the total area would collapse to 0 and f would stop being a probability distribution. Normalisation (∫ f = 1 ) is forced at all T , which is precisely why the height must run to infinity as the width runs to zero. Physically: a frozen gas has every molecule essentially at rest.
Step 2 (T → ∞ ). v p → ∞ ; the peak slides right without bound and the curve flattens (its area must stay 1, so a wider curve must be lower).
Why this step? Hotter = faster and broader, as the parent's Forecast-then-Verify predicted.
Step 3. Sanity number: doubling T multiplies every landmark speed by 2 ≈ 1.414 .
Why this step? v ∝ T means a 4 × temperature jump only doubles speeds — heating is an inefficient way to speed molecules up.
Verify: 2 = 1.41421 ✓. In figure s03 the red curve (2 T ) sits to the right of and lower than the black (T ) curve; both enclose the same area 1, confirming the "wider means lower" trade-off ✓.
Figure s03: Two speed distributions at temperature T (black) and 2 T (red). Heating pushes the peak right and lowers it; both curves keep unit area.
300 K , how much faster is the mean speed of helium (He, m = 4 u) than that of xenon (Xe, m = 131 u)?
Forecast: Both feel the same temperature, so same average energy — but the light one must move much faster to carry it. Guess the ratio.
Step 1. In ⟨ v ⟩ = 8 k B T / π m only m differs between the gases. So
⟨ v ⟩ X e ⟨ v ⟩ H e = m H e m X e .
Why this step? T and all constants cancel — the ratio depends only on the mass ratio.
Step 2. 131/4 = 32.75 = 5.72 .
Why this step? Speed scales as 1/ m : 33× heavier ⇒ ~5.7× slower.
Verify: 32.75 = 5.7227 ✓. Physically, equipartition gives both the same 2 3 k B T energy, so v ∝ 1/ m — helium leaks out of balloons far faster than xenon would. (See Effusion and Graham's law .)
Worked example Can hydrogen escape Earth's atmosphere, but not oxygen?
Earth's escape speed is v esc = 1.12 × 1 0 4 m/s . Upper-atmosphere temperature ≈ 1000 K . Compare v r m s for H₂ (m = 2 u) and O₂ (m = 32 u). A gas leaks away over geological time once v esc ≲ 6 v r m s .
Forecast: Light H₂ is fast — guess it can leak. Heavy O₂ is slow — guess it stays.
Step 1. H₂: m = 2 × 1.66 × 1 0 − 27 = 3.32 × 1 0 − 27 kg.
v r m s = 3.32 × 1 0 − 27 3 ( 1.38 × 1 0 − 23 ) ( 1000 ) = 1.247 × 1 0 7 ≈ 3530 m/s .
Why this step? v r m s (factor 3) is the fairest "energy speed" for an escape argument.
Step 2. O₂: m = 16 × heavier, so v r m s is 16 = 4 × smaller: 3530/4 ≈ 883 m/s .
Why this step? Reuse the 1/ m scaling instead of recomputing from scratch.
Step 3. Compare to threshold v esc /6 = 1.12 × 1 0 4 /6 = 1867 m/s.
H₂: 3530 > 1867 ⇒ its fast tail escapes. Leaks away. ✓ forecast
O₂: 883 < 1867 ⇒ tail negligible at v esc . Retained. ✓ forecast
Why this step? Escape is governed by the tail (Ex 4), and the tail sits at a fixed multiple of v r m s .
Verify: 1.247 × 1 0 7 = 3531 m/s ✓; 3531/4 = 883 m/s ✓. This is exactly why Earth kept its O₂ and N₂ but lost nearly all its free hydrogen.
⟨ v ⟩ / v p is a pure number, and find it.
Forecast: From the parent's ordering v p < ⟨ v ⟩ , guess a number slightly above 1.
Step 1. Write both with the common factor k B T / m :
v p = 2 m k B T , ⟨ v ⟩ = π 8 m k B T .
Why this step? Factoring out the shared physics makes the cancellation obvious.
Step 2. Divide:
v p ⟨ v ⟩ = 2 8/ π = π 4 = π 2 ≈ 1.128.
Why this step? k B T / m cancels completely — the ratio is the same for every gas at every temperature.
Verify: 2/ π = 1.1284 ✓, and 1 < 1.128 , consistent with v p < ⟨ v ⟩ ✓.
Worked example What fraction of molecules have speeds between
v p and 2 v p ?
Forecast: This band straddles the hump's peak and part of the falling side — guess a sizeable chunk, maybe half.
Step 1. Non-dimensionalise with u = v / v p , so v = u v p and d v = v p d u , and the exponent m v 2 /2 k B T = u 2 . Then f ( v ) d v ∝ u 2 e − u 2 d u and, using ∫ 0 ∞ u 2 e − u 2 d u = π /4 for normalisation,
fraction = ∫ 0 ∞ u 2 e − u 2 d u ∫ 1 2 u 2 e − u 2 d u = π 4 ∫ 1 2 u 2 e − u 2 d u .
Why this step? Scaling removes m , T ; the answer is universal (holds for any gas at any T ). See Gaussian integrals .
Step 2. Evaluate the finite integral using the antiderivative ∫ u 2 e − u 2 d u = 4 π erf ( u ) − 2 u e − u 2 (with erf as defined at the top):
∫ 1 2 u 2 e − u 2 d u = [ 4 π erf ( u ) − 2 u e − u 2 ] 1 2 = 0.2332.
Why this step? A closed antiderivative avoids numerical guessing; erf handles the Gaussian part.
Step 3. Multiply by the normalisation prefactor to get the final fraction:
fraction = π 4 ( 0.2332 ) = 1.7725 4 ( 0.2332 ) = 0.526 ≈ 53%.
Why this step? The prefactor 4/ π is the reciprocal of the normalising integral π /4 ; multiplying converts the raw integral into a fraction of all molecules .
Verify: In figure s04 the red shaded band from v p to 2 v p visibly covers about half the total area under the curve, matching 0.53 ✓. (Our "maybe half" forecast was right on the money — the band brackets the peak, so it captures the bulk of the molecules.)
Figure s04: Speed distribution vs v / v p ; the red-shaded region between v p and 2 v p is ~53% of the total area, marked by dashed lines at u = 1 and u = 2 .
Recall Which cell is each example?
A→Ex1 (plug-in) · B→Ex2 (signs, both tails) · C→Ex3 (v = 0 ) · D→Ex4 (v → ∞ ) · E→Ex5 (T → 0 , ∞ ) · F→Ex6 (mass extremes) · G→Ex7 (word problem) · H→Ex8 (ratio) · I→Ex9 (finite band).
Why is f ( 0 ) = 0 even though the Boltzmann factor is maximal there? The geometric shell factor v 2 → 0 : a sphere of radius 0 has no volume, so no velocity vectors have exactly zero magnitude.
For two gases at the same T , how do their mean speeds compare? ⟨ v ⟩ ∝ 1/ m — the mass ratio's inverse square root;
T cancels.
Is ⟨ v ⟩ / v p gas-dependent? No — it equals
2/ π ≈ 1.128 for every ideal gas at every temperature.
As T → 0 , what happens to f ( v ) ? It collapses to a Dirac delta spike at
v = 0 ; the diverging prefactor
∝ T − 3/2 keeps the area equal to 1 as the width
∝ T shrinks.
What does erfc ( z ) measure? The fraction of a Gaussian's area lying in the tail beyond z , i.e. erfc ( z ) = 1 − erf ( z ) .