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Unit B3 · SolutionsUnit B3 · 解析

Gas Laws · Solutions气体定律 · 解析

Companion to the IB-Style Practice SetIB 风格练习题的解析配套

MEDIUM HARD Paper 1 Paper 1B Paper 2 HL ONLY

Syllabus B3.1 to B3.6考纲 B3.1 至 B3.6PHYSICS HL



PART I  ·  PAPER 1 STYLE第一部分  ·  第一卷风格Short structured · 30 marks短结构题 · 30 分

Worked Solutions详细解析

Q1MEDIUMPaper 1mole, molar mass, Avogadro count摩尔、摩尔质量、阿伏伽德罗计数[4 marks]

$88\ \mathrm{g}$ of $\mathrm{CO_2}$, $M = 44\ \mathrm{g\,mol^{-1}}$. (a) amount of substance; (b) number of molecules.$88\ \mathrm{g}$ 的 $\mathrm{CO_2}$,$M = 44\ \mathrm{g\,mol^{-1}}$。(a) 物质的量;(b) 分子数。

Answers:答案:  (a) $n = 2.0\ \mathrm{mol}$  ·  (b) $N \approx 1.2\times 10^{24}$ molecules

(a) Amount of substance M1·A1

The amount of substance is mass divided by molar mass: $n = m/M$. (M1)

$$ n = \frac{88}{44} = 2.0\ \mathrm{mol}. $$

(A1)

(b) Number of molecules M1·A1

Multiply the amount of substance by the Avogadro constant: $N = n N_A$. (M1)

$$ N = (2.0)(6.02\times 10^{23}) = 1.2\times 10^{24}\ \text{molecules}. $$

(A1)

Insight. Keep the chain $m \to n \to N$ separate in your head: divide by molar mass to reach moles, then multiply by $N_A$ to reach a molecule count. The molar mass in $\mathrm{g\,mol^{-1}}$ pairs naturally with mass in grams, so no kilogram conversion is needed here. Only convert $M$ to $\mathrm{kg\,mol^{-1}}$ when you later need the mass of a single molecule in SI units, as in the kinetic-theory questions.

(a) 物质的量 M1·A1

物质的量等于质量除以摩尔质量:$n = m/M$。(M1)

$$ n = \frac{88}{44} = 2.0\ \mathrm{mol}. $$

(A1)

(b) 分子数 M1·A1

把物质的量乘以阿伏伽德罗常数:$N = n N_A$。(M1)

$$ N = (2.0)(6.02\times 10^{23}) = 1.2\times 10^{24}\ \text{个分子}. $$

(A1)

要点。把链条 $m \to n \to N$ 在脑中分清:除以摩尔质量得摩尔,再乘以 $N_A$ 得分子数。以 $\mathrm{g\,mol^{-1}}$ 为单位的摩尔质量天然与以克为单位的质量配对,此处无需换成千克。只有当随后需要以 SI 单位求单个分子的质量时(如动理论题),才把 $M$ 换成 $\mathrm{kg\,mol^{-1}}$。
Q2MEDIUMPaper 1Boyle's law, isothermal change玻意耳定律,等温变化[4 marks]

Fixed mass at $1.0\times 10^{5}\ \mathrm{Pa}$, $0.024\ \mathrm{m^{3}}$, compressed isothermally to $0.0060\ \mathrm{m^{3}}$. (a) which law; (b) new pressure; (c) internal energy.一定质量气体在 $1.0\times 10^{5}\ \mathrm{Pa}$、$0.024\ \mathrm{m^{3}}$,等温压缩到 $0.0060\ \mathrm{m^{3}}$。(a) 何定律;(b) 新压强;(c) 内能。

Answers:答案:  (a) Boyle's law, constant $T$  ·  (b) $p_2 = 4.0\times 10^{5}\ \mathrm{Pa}$  ·  (c) internal energy unchanged

(a) Identifying the law B1

The change is isothermal (constant temperature) for a fixed mass of gas, so Boyle's law applies: $pV = \text{constant}$. (B1)

(b) New pressure M1·A1

Apply $p_1 V_1 = p_2 V_2$, so $p_2 = p_1 V_1 / V_2$. (M1)

$$ p_2 = \frac{(1.0\times 10^{5})(0.024)}{0.0060} = 4.0\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(c) Internal energy B1

For an ideal gas the internal energy depends only on temperature. The change is isothermal, so the internal energy is unchanged. (B1)

Insight. The word "isothermal" is the marker's signal to set $T$ constant and reach straight for Boyle's law, and it is also the justification for part (c): since $U \propto T$ for an ideal gas, constant $T$ forces constant $U$, no matter how the pressure and volume trade off. Volume fell by a factor of four, so pressure rose by exactly four. Always check that $p$ and $V$ move in opposite directions in a Boyle's-law step, a quick guard against inverting the ratio.

(a) 判定定律 B1

该变化对固定质量气体为等温(温度恒定),故适用玻意耳定律:$pV = \text{常数}$。(B1)

(b) 新压强 M1·A1

用 $p_1 V_1 = p_2 V_2$,故 $p_2 = p_1 V_1 / V_2$。(M1)

$$ p_2 = \frac{(1.0\times 10^{5})(0.024)}{0.0060} = 4.0\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(c) 内能 B1

理想气体的内能只依赖于温度。该变化为等温,故内能不变。(B1)

要点。"等温"一词是阅卷的信号,提示令 $T$ 恒定并直接用玻意耳定律,它同时也是 (c) 的理由:因理想气体 $U \propto T$,温度恒定即迫使内能恒定,无论压强与体积如何此消彼长。体积减为 $1/4$,压强便恰增至 4 倍。在玻意耳步骤中始终核对 $p$ 与 $V$ 反向变化,可快速防止比值写反。
Q3MEDIUMPaper 1ideal gas equation + Gay-Lussac理想气体方程与盖-吕萨克[6 marks]

Rigid container of gas at $1.5\times 10^{5}\ \mathrm{Pa}$, $300\ \mathrm{K}$. (a) cooled to $250\ \mathrm{K}$, find new pressure; (b) separately, $0.50\ \mathrm{mol}$ ideal gas at $1.0\times 10^{5}\ \mathrm{Pa}$, $300\ \mathrm{K}$, find volume.刚性容器气体在 $1.5\times 10^{5}\ \mathrm{Pa}$、$300\ \mathrm{K}$。(a) 冷却到 $250\ \mathrm{K}$,求新压强;(b) 另取 $0.50\ \mathrm{mol}$ 理想气体于 $1.0\times 10^{5}\ \mathrm{Pa}$、$300\ \mathrm{K}$,求体积。

Answers:答案:  (a) $p_2 = 1.25\times 10^{5}\ \mathrm{Pa}$  ·  (b) $V \approx 0.012\ \mathrm{m^{3}}$

(a) New pressure at constant volume M1·M1·A1

A rigid container fixes the volume, so Gay-Lussac's law applies: $p/T = \text{constant}$, i.e. $p_1/T_1 = p_2/T_2$. (M1)

Rearrange for $p_2 = p_1 (T_2/T_1)$: (M1)

$$ p_2 = (1.5\times 10^{5})\frac{250}{300} = 1.25\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(b) Volume from the ideal gas equation M1·M1·A1

Use $pV = nRT$ rearranged to $V = nRT/p$. The temperature is already $300\ \mathrm{K}$. (M1)

$$ V = \frac{(0.50)(8.31)(300)}{1.0\times 10^{5}}. $$

(M1 for substitution)

$$ V = \frac{1246.5}{1.0\times 10^{5}} = 0.0125\ \mathrm{m^{3}} \approx 0.012\ \mathrm{m^{3}}. $$

(A1)

Insight. Both parts come from one master equation, $pV = nRT$. In part (a) the amount $n$ and the volume $V$ are fixed, so $nR/V$ is constant and the equation collapses to $p \propto T$, which is exactly Gay-Lussac's law. Naming the empirical law is worth a mark, but recognising it as a special case of $pV = nRT$ stops you from memorising three separate laws. Temperatures were given in kelvin here, removing the most common trap, but always check the units before substituting.

(a) 恒容下的新压强 M1·M1·A1

刚性容器使体积固定,故适用盖-吕萨克定律:$p/T = \text{常数}$,即 $p_1/T_1 = p_2/T_2$。(M1)

解出 $p_2 = p_1 (T_2/T_1)$:(M1)

$$ p_2 = (1.5\times 10^{5})\frac{250}{300} = 1.25\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(b) 由理想气体方程求体积 M1·M1·A1

用 $pV = nRT$ 改写为 $V = nRT/p$。温度已是 $300\ \mathrm{K}$。(M1)

$$ V = \frac{(0.50)(8.31)(300)}{1.0\times 10^{5}}. $$

(代入得 M1)

$$ V = \frac{1246.5}{1.0\times 10^{5}} = 0.0125\ \mathrm{m^{3}} \approx 0.012\ \mathrm{m^{3}}. $$

(A1)

要点。两小问都源自同一主方程 $pV = nRT$。在 (a) 中气体量 $n$ 与体积 $V$ 固定,故 $nR/V$ 为常数,方程化为 $p \propto T$,这正是盖-吕萨克定律。写出经验定律名称值一分,但把它看作 $pV = nRT$ 的特例可免去死记三条独立定律。此处温度已给为开尔文,避开了最常见的陷阱,但代入前务必核对单位。
Q4HARDPaper 1kinetic theory: pressure + assumptions动理论:压强与假设[8 marks]

$pV = \tfrac{1}{3} N m \overline{c^{2}}$. (a) two ideal-gas assumptions; (b) why a gas exerts pressure; (c) compute $p$ from $n_V = 2.7\times 10^{25}\ \mathrm{m^{-3}}$, $m = 4.7\times 10^{-26}\ \mathrm{kg}$, $\overline{c^{2}} = 2.6\times 10^{5}\ \mathrm{m^{2}\,s^{-2}}$; (d) effect of doubling $n_V$.$pV = \tfrac{1}{3} N m \overline{c^{2}}$。(a) 两条理想气体假设;(b) 气体为何产生压强;(c) 由 $n_V = 2.7\times 10^{25}\ \mathrm{m^{-3}}$、$m = 4.7\times 10^{-26}\ \mathrm{kg}$、$\overline{c^{2}} = 2.6\times 10^{5}\ \mathrm{m^{2}\,s^{-2}}$ 算 $p$;(d) $n_V$ 翻倍的影响。

Answers:答案:  (a) e.g. point molecules; no forces except in collisions  ·  (b) momentum change at the walls  ·  (c) $p \approx 1.1\times 10^{5}\ \mathrm{Pa}$  ·  (d) pressure doubles

(a) Two assumptions A1·A1

Any two of: molecules are point particles whose own volume is negligible compared with the container; there are no intermolecular forces except during collisions; collisions are perfectly elastic; molecular motion is random; the time of a collision is negligible compared with the time between collisions. (A1·A1)

(b) Why a gas exerts pressure M1·A1

Molecules move randomly and collide with the container walls. Each elastic collision reverses the molecule's momentum component, so the wall exerts an impulse on the molecule and, by Newton's third law, the molecule exerts an equal force on the wall. (M1)

The pressure is the total rate of momentum transfer per unit area summed over the very large number of such collisions. (A1)

(c) Pressure from the model M1·M1·A1

Use $p = \tfrac{1}{3} n_V m \overline{c^{2}}$. (M1)

$$ p = \tfrac{1}{3}(2.7\times 10^{25})(4.7\times 10^{-26})(2.6\times 10^{5}). $$

(M1 for substitution)

$$ p \approx 1.1\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(d) Doubling the number density B1

Since $p \propto n_V$ at constant $\overline{c^{2}}$ (constant temperature), doubling the number density doubles the pressure. (B1)

Insight. Pressure in kinetic theory is a momentum-transfer rate, not a static push; the factor $\tfrac{1}{3}$ comes from sharing the mean-square speed equally between the three perpendicular directions. When substituting, the molecular mass must be in kilograms and the mean-square speed in $\mathrm{m^{2}\,s^{-2}}$, so the product lands in pascals. Part (d) is fast if you read $p = \tfrac{1}{3} n_V m \overline{c^{2}}$ as a direct proportionality: number density sets how many collisions per second, and at fixed temperature each collision carries the same average momentum.

(a) 两条假设 A1·A1

以下任取两条:分子为质点,其自身体积相对容器可忽略;除碰撞瞬间外无分子间作用力;碰撞完全弹性;分子运动随机;碰撞持续时间相对碰撞间隔可忽略。(A1·A1)

(b) 气体为何产生压强 M1·A1

分子随机运动并与器壁碰撞。每次弹性碰撞使分子的动量分量反向,故器壁对分子施加冲量,由牛顿第三定律,分子对器壁施加等大的力。(M1)

压强即对大量这类碰撞求和后单位面积上动量传递的总速率。(A1)

(c) 由模型求压强 M1·M1·A1

用 $p = \tfrac{1}{3} n_V m \overline{c^{2}}$。(M1)

$$ p = \tfrac{1}{3}(2.7\times 10^{25})(4.7\times 10^{-26})(2.6\times 10^{5}). $$

(代入得 M1)

$$ p \approx 1.1\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(d) 数密度翻倍 B1

在 $\overline{c^{2}}$ 不变(温度不变)时 $p \propto n_V$,故数密度翻倍则压强翻倍。(B1)

要点。动理论中的压强是动量传递的速率,而非静态的推压;因子 $\tfrac{1}{3}$ 来自把均方速率平均分配到三个互相垂直的方向。代入时分子质量须以千克计、均方速率以 $\mathrm{m^{2}\,s^{-2}}$ 计,乘积才落在帕斯卡。若把 $p = \tfrac{1}{3} n_V m \overline{c^{2}}$ 读作直接正比关系,(d) 就很快:数密度决定每秒碰撞次数,而恒温下每次碰撞携带相同的平均动量。
Q5HARDPaper 1HL ONLYmean KE, internal energy, $T \propto \bar{E}_k$平均动能、内能、$T \propto \bar{E}_k$[8 marks]

Monatomic ideal gas at $400\ \mathrm{K}$. (a) show $\bar{E}_k = \tfrac{3}{2} k_B T$; (b) mean KE per molecule; (c) internal energy of $3.0\ \mathrm{mol}$ and why it is purely kinetic.单原子理想气体于 $400\ \mathrm{K}$。(a) 证明 $\bar{E}_k = \tfrac{3}{2} k_B T$;(b) 每分子平均动能;(c) $3.0\ \mathrm{mol}$ 的内能及其为何纯为动能。

Answers:答案:  (a) $\bar{E}_k = \tfrac{3}{2} k_B T$  ·  (b) $\bar{E}_k \approx 8.3\times 10^{-21}\ \mathrm{J}$  ·  (c) $U \approx 1.5\times 10^{4}\ \mathrm{J}$

(a) Deriving $\bar{E}_k = \tfrac{3}{2} k_B T$ M1·M1·A1

Kinetic theory gives $pV = \tfrac{1}{3} N m \overline{c^{2}}$; the ideal gas law gives $pV = N k_B T$. Equate the two expressions for $pV$: (M1)

$$ \tfrac{1}{3} N m \overline{c^{2}} = N k_B T \;\Rightarrow\; \tfrac{1}{3} m \overline{c^{2}} = k_B T. $$

Multiply both sides by $\tfrac{3}{2}$ so the left side becomes the mean translational kinetic energy $\tfrac{1}{2} m \overline{c^{2}}$: (M1)

$$ \bar{E}_k = \tfrac{1}{2} m \overline{c^{2}} = \tfrac{3}{2} k_B T. $$

(A1)

(b) Mean kinetic energy per molecule M1·A1

Substitute $T = 400\ \mathrm{K}$ into $\bar{E}_k = \tfrac{3}{2} k_B T$: (M1)

$$ \bar{E}_k = \tfrac{3}{2}(1.38\times 10^{-23})(400) \approx 8.3\times 10^{-21}\ \mathrm{J}. $$

(A1)

(c) Internal energy of the sample M1·A1·B1

For a monatomic ideal gas $U = \tfrac{3}{2} n R T$: (M1)

$$ U = \tfrac{3}{2}(3.0)(8.31)(400) \approx 1.5\times 10^{4}\ \mathrm{J}. $$

(A1)

A monatomic gas has no rotational or vibrational modes and the ideal model has no intermolecular potential energy, so the internal energy is purely the sum of the molecules' translational kinetic energies. (B1)

Insight. This derivation is the conceptual heart of B3.5: equating the two faces of $pV$ identifies absolute temperature as a direct measure of mean molecular kinetic energy, independent of the gas's identity. The examiner expects the explicit "multiply by $\tfrac{3}{2}$" step that turns $\tfrac{1}{3} m \overline{c^{2}}$ into $\tfrac{1}{2} m \overline{c^{2}}$; skipping it loses the method mark even if the final formula is quoted correctly. Note that $\bar{E}_k$ uses $k_B$ per molecule while $U$ uses $R$ per mole, the two linked by $R = N_A k_B$.

(a) 推导 $\bar{E}_k = \tfrac{3}{2} k_B T$ M1·M1·A1

动理论给出 $pV = \tfrac{1}{3} N m \overline{c^{2}}$;理想气体定律给出 $pV = N k_B T$。令 $pV$ 的两式相等:(M1)

$$ \tfrac{1}{3} N m \overline{c^{2}} = N k_B T \;\Rightarrow\; \tfrac{1}{3} m \overline{c^{2}} = k_B T. $$

两边乘以 $\tfrac{3}{2}$,使左边化为平均平动动能 $\tfrac{1}{2} m \overline{c^{2}}$:(M1)

$$ \bar{E}_k = \tfrac{1}{2} m \overline{c^{2}} = \tfrac{3}{2} k_B T. $$

(A1)

(b) 每分子平均动能 M1·A1

把 $T = 400\ \mathrm{K}$ 代入 $\bar{E}_k = \tfrac{3}{2} k_B T$:(M1)

$$ \bar{E}_k = \tfrac{3}{2}(1.38\times 10^{-23})(400) \approx 8.3\times 10^{-21}\ \mathrm{J}. $$

(A1)

(c) 样品的内能 M1·A1·B1

单原子理想气体 $U = \tfrac{3}{2} n R T$:(M1)

$$ U = \tfrac{3}{2}(3.0)(8.31)(400) \approx 1.5\times 10^{4}\ \mathrm{J}. $$

(A1)

单原子气体没有转动或振动自由度,且理想模型无分子间势能,故内能纯为各分子平动动能之和。(B1)

要点。这一推导是 B3.5 的概念核心:令 $pV$ 的两种形式相等,把绝对温度等同为平均分子动能的直接量度,与气体种类无关。阅卷要求写出明确的"乘以 $\tfrac{3}{2}$"步骤,把 $\tfrac{1}{3} m \overline{c^{2}}$ 变为 $\tfrac{1}{2} m \overline{c^{2}}$;即使末式抄对,省略此步也会失方法分。注意 $\bar{E}_k$ 用每分子的 $k_B$,而 $U$ 用每摩尔的 $R$,两者由 $R = N_A k_B$ 联系。
PART II  ·  PAPER 1B / DATA ANALYSIS第二部分  ·  第一卷 B / 数据分析Graphs · data · uncertainties · 22 marks图像 · 数据 · 不确定度 · 22 分

Worked Solutions详细解析

Q6HARDPaper 1BBoyle's law: $p$ vs $1/V$ + uncertainty玻意耳定律:$p$ 对 $1/V$ 与不确定度[10 marks]

Constant-$T$ compression; $p$ vs $1/V$ data given. (a) show $p$ vs $1/V$ is linear through the origin and state the gradient; (b) gradient and the value of $pV$; (c) percentage uncertainty in the $2.40\times 10^{5}\ \mathrm{Pa}$ reading ($\pm 0.05\times 10^{5}$); (d) why points curve at high pressure.恒温压缩;给出 $p$ 对 $1/V$ 的数据。(a) 证明 $p$ 对 $1/V$ 为过原点直线并说明斜率;(b) 斜率与 $pV$ 值;(c) $2.40\times 10^{5}\ \mathrm{Pa}$ 读数($\pm 0.05\times 10^{5}$)的百分比不确定度;(d) 高压下点为何弯曲。

Answers:答案:  (a) $p = (pV)\cdot\tfrac{1}{V}$, gradient $= pV$  ·  (b) gradient $= 2.4\times 10^{3}\ \mathrm{J}$, so $pV = 2.4\times 10^{3}\ \mathrm{J}$  ·  (c) $\approx 2\%$  ·  (d) real-gas deviation (finite molecular volume / attractions)

(a) Why $p$ vs $1/V$ is linear through the origin M1·A1·A1

Boyle's law at constant temperature and fixed mass: $pV = \text{constant}$. Rearrange to make $p$ the subject: (M1)

$$ p = (pV)\cdot\frac{1}{V}. $$

This has the form $p = (\text{gradient})\times (1/V)$ with no intercept, so a plot of $p$ against $1/V$ is a straight line through the origin. (A1)

Comparing with $y = mx$, the gradient equals the constant $pV$. (A1)

(b) Gradient and the value of $pV$ M1·A1·A1

Read the gradient from two well-separated points, e.g. $(25,\,0.60\times 10^{5})$ and $(100,\,2.40\times 10^{5})$: (M1)

$$ \text{gradient} = \frac{(2.40 - 0.60)\times 10^{5}}{100 - 25} = \frac{1.80\times 10^{5}}{75} = 2.4\times 10^{3}\ \mathrm{J}. $$

(A1)

Since the gradient is the Boyle's-law constant, $pV = 2.4\times 10^{3}\ \mathrm{J}$. (A1)

(c) Percentage uncertainty M1·A1

Divide the absolute uncertainty by the reading: (M1)

$$ \frac{0.05\times 10^{5}}{2.40\times 10^{5}}\times 100\% \approx 2.1\% \approx 2\%. $$

(A1)

(d) Why the points curve at high pressure B1·R1

At very high pressure the gas is no longer ideal: the finite volume of the molecules themselves becomes significant and intermolecular attractions are no longer negligible. (B1)

Boyle's law assumes ideal behaviour, so the real data deviate from the straight line as these assumptions fail. (R1)

Insight. Plotting $p$ against $1/V$ rather than against $V$ converts the hyperbola of Boyle's law into a straight line, and a straight-line gradient averages out random scatter far better than any single $(p, V)$ product. The marker awards the gradient only when it is read from widely separated points or the line of best fit, never from one point divided out. The curvature in part (d) is the experimental fingerprint of real-gas behaviour, the same physics that makes $pV/(nRT)$ drift away from 1 at high pressure.

(a) 为何 $p$ 对 $1/V$ 为过原点直线 M1·A1·A1

恒温、固定质量下的玻意耳定律:$pV = \text{常数}$。改写为以 $p$ 为主体:(M1)

$$ p = (pV)\cdot\frac{1}{V}. $$

此式形如 $p = (\text{斜率})\times (1/V)$,无截距,故 $p$ 对 $1/V$ 作图为过原点的直线。(A1)

与 $y = mx$ 比较,斜率等于常数 $pV$。(A1)

(b) 斜率与 $pV$ 值 M1·A1·A1

用相距较远的两点读斜率,如 $(25,\,0.60\times 10^{5})$ 与 $(100,\,2.40\times 10^{5})$:(M1)

$$ \text{斜率} = \frac{(2.40 - 0.60)\times 10^{5}}{100 - 25} = \frac{1.80\times 10^{5}}{75} = 2.4\times 10^{3}\ \mathrm{J}. $$

(A1)

因斜率即玻意耳定律常数,故 $pV = 2.4\times 10^{3}\ \mathrm{J}$。(A1)

(c) 百分比不确定度 M1·A1

用绝对不确定度除以读数:(M1)

$$ \frac{0.05\times 10^{5}}{2.40\times 10^{5}}\times 100\% \approx 2.1\% \approx 2\%. $$

(A1)

(d) 高压下点为何弯曲 B1·R1

在极高压下气体不再理想:分子自身的有限体积变得显著,分子间吸引也不再可忽略。(B1)

玻意耳定律假设理想行为,故当这些假设失效时实验数据偏离直线。(R1)

要点。以 $p$ 对 $1/V$ 而非对 $V$ 作图,把玻意耳定律的双曲线化为直线,而直线斜率比任何单个 $(p, V)$ 乘积都更能平均掉随机散布。只有从相距较远的点或最佳拟合线读出斜率才给分,绝不用单点相除。(d) 中的弯曲是真实气体行为的实验指纹,与高压下使 $pV/(nRT)$ 偏离 1 的物理同源。
Q7HARDPaper 1B$pV$ vs $T$: gradient gives $nR$$pV$ 对 $T$:斜率给出 $nR$[12 marks]

Fixed amount of ideal gas; $pV$ (J) vs $T$ (K) data given. (a) show $pV$ vs $T$ is linear through the origin and state the gradient; (b) gradient from first and last points; (c) amount of substance $n$; (d) why through the origin and meaning of $pV$ at $T = 0$; (e) effect of recording $T$ in Celsius.固定量理想气体;给出 $pV$(J)对 $T$(K)的数据。(a) 证明 $pV$ 对 $T$ 为过原点直线并说明斜率;(b) 由首末点求斜率;(c) 物质的量 $n$;(d) 为何过原点及 $T = 0$ 处 $pV$ 的含义;(e) 用摄氏度记温的影响。

Answers:答案:  (a) $pV = (nR)\,T$, gradient $= nR$  ·  (b) gradient $\approx 4.2\ \mathrm{J\,K^{-1}}$  ·  (c) $n \approx 0.50\ \mathrm{mol}$  ·  (d) $pV \to 0$ as $T \to 0\ \mathrm{K}$  ·  (e) line shifts, no longer through the origin

(a) Why $pV$ vs $T$ is linear through the origin M1·A1·A1

The ideal gas equation is $pV = nRT$. For a fixed amount of gas $n$ is constant, so $nR$ is a constant: (M1)

$$ pV = (nR)\,T. $$

This has the form $pV = (\text{gradient})\times T$ with no intercept, so a plot of $pV$ against $T$ (in kelvin) is a straight line through the origin. (A1)

Comparing with $y = mx$, the gradient is $nR$. (A1)

(b) Gradient from the endpoints M1·M1·A1

Use the first and last data points $(200,\,830)$ and $(500,\,2080)$: (M1)

$$ \text{gradient} = \frac{2080 - 830}{500 - 200}. $$

(M1 for substitution)

$$ \text{gradient} = \frac{1250}{300} \approx 4.2\ \mathrm{J\,K^{-1}}. $$

(A1)

(c) Amount of substance M1·A1

The gradient equals $nR$, so $n = \text{gradient}/R$: (M1)

$$ n = \frac{4.2}{8.31} \approx 0.50\ \mathrm{mol}. $$

(A1)

(d) Through the origin and $pV$ at $T = 0$ B1·R1

Because $pV = nRT$ has no constant term, $pV$ must tend to zero as $T$ tends to $0\ \mathrm{K}$, which is why the line passes through the origin. (B1)

A value $pV = 0$ at $T = 0\ \mathrm{K}$ represents the molecules having zero average translational kinetic energy, so they exert no pressure: absolute zero. (R1)

(e) Recording $T$ in Celsius A1·R1

Using Celsius shifts every temperature by $273$, so the line would no longer pass through the origin: it would cross the $pV$ axis at a positive intercept and the temperature axis near $-273\ ^\circ\mathrm{C}$. (A1)

The line stays straight with the same gradient $nR$, but the proportionality $pV \propto T$ holds only when $T$ is the absolute (kelvin) temperature. (R1)

Insight. Reading $nR$ off the gradient of a $pV$-vs-$T$ line is the cleanest way to find an unknown amount of gas, because the gradient pools every data point instead of trusting one substitution. The intercept is diagnostic: a line through the origin confirms kelvin temperatures and ideal behaviour, while a positive $pV$ intercept is the signature of a Celsius axis, exactly the construction that originally located absolute zero. Note the gradient is $nR$, not $n$, so dividing by $R$ is the final, easily forgotten step.

(a) 为何 $pV$ 对 $T$ 为过原点直线 M1·A1·A1

理想气体方程为 $pV = nRT$。对固定气体量 $n$ 为常数,故 $nR$ 为常数:(M1)

$$ pV = (nR)\,T. $$

此式形如 $pV = (\text{斜率})\times T$,无截距,故 $pV$ 对 $T$(开尔文)作图为过原点的直线。(A1)

与 $y = mx$ 比较,斜率为 $nR$。(A1)

(b) 由首末点求斜率 M1·M1·A1

用首末两点 $(200,\,830)$ 与 $(500,\,2080)$:(M1)

$$ \text{斜率} = \frac{2080 - 830}{500 - 200}. $$

(代入得 M1)

$$ \text{斜率} = \frac{1250}{300} \approx 4.2\ \mathrm{J\,K^{-1}}. $$

(A1)

(c) 物质的量 M1·A1

斜率等于 $nR$,故 $n = \text{斜率}/R$:(M1)

$$ n = \frac{4.2}{8.31} \approx 0.50\ \mathrm{mol}. $$

(A1)

(d) 过原点与 $T = 0$ 处的 $pV$ B1·R1

因 $pV = nRT$ 无常数项,当 $T$ 趋于 $0\ \mathrm{K}$ 时 $pV$ 必趋于零,这正是直线过原点的原因。(B1)

$T = 0\ \mathrm{K}$ 处 $pV = 0$ 表示分子的平均平动动能为零,因而不产生压强:即绝对零度。(R1)

(e) 用摄氏度记温 A1·R1

用摄氏度会把每个温度平移 $273$,故直线不再过原点:它将在 $pV$ 轴交于一个正截距,并在 $-273\ ^\circ\mathrm{C}$ 附近交温度轴。(A1)

直线仍为直线、斜率仍为 $nR$,但比例关系 $pV \propto T$ 仅当 $T$ 取绝对(开尔文)温度时成立。(R1)

要点。从 $pV$ 对 $T$ 直线的斜率读出 $nR$,是求未知气体量最干净的方法,因为斜率汇集了所有数据点而非依赖单次代入。截距具有诊断意义:过原点的直线确认了开尔文温度与理想行为,而正的 $pV$ 截距是摄氏轴的标志,这正是当年定位绝对零度的构造。注意斜率是 $nR$ 而非 $n$,因此除以 $R$ 是最后一步,且极易遗漏。
PART III  ·  PAPER 2 STYLE第三部分  ·  第二卷风格Extended structured · 30 marks长结构题 · 30 分

Worked Solutions详细解析

Q8HARDPaper 2moles from $pV=nRT$ then heating由 $pV=nRT$ 求摩尔再加热[12 marks]

Rigid cylinder $0.025\ \mathrm{m^{3}}$, monatomic ideal gas at $2.0\times 10^{5}\ \mathrm{Pa}$, $300\ \mathrm{K}$. (a) moles; (b) number of molecules; (c) new pressure heated to $500\ \mathrm{K}$ at constant $V$; (d) increase in internal energy $300 \to 500\ \mathrm{K}$; (e) change in mean KE per molecule.刚性气缸 $0.025\ \mathrm{m^{3}}$,单原子理想气体于 $2.0\times 10^{5}\ \mathrm{Pa}$、$300\ \mathrm{K}$。(a) 摩尔数;(b) 分子数;(c) 恒容加热到 $500\ \mathrm{K}$ 的新压强;(d) $300 \to 500\ \mathrm{K}$ 内能增量;(e) 每分子平均动能的变化。

Answers:答案:  (a) $n \approx 2.0\ \mathrm{mol}$  ·  (b) $N \approx 1.2\times 10^{24}$  ·  (c) $p_2 \approx 3.3\times 10^{5}\ \mathrm{Pa}$  ·  (d) $\Delta U \approx 5.0\times 10^{3}\ \mathrm{J}$  ·  (e) increases by a factor of $5/3$

(a) Amount of substance M1·M1·A1

Use $pV = nRT$, so $n = pV/(RT)$ with $T = 300\ \mathrm{K}$. (M1)

$$ n = \frac{(2.0\times 10^{5})(0.025)}{(8.31)(300)}. $$

(M1 for substitution)

$$ n = \frac{5000}{2493} \approx 2.0\ \mathrm{mol}. $$

(A1)

(b) Number of molecules M1·A1

$N = n N_A$: (M1)

$$ N = (2.0)(6.02\times 10^{23}) \approx 1.2\times 10^{24}. $$

(A1)

(c) New pressure at constant volume M1·A1

Constant volume, so $p \propto T$ (Gay-Lussac): $p_2 = p_1 (T_2/T_1)$. (M1)

$$ p_2 = (2.0\times 10^{5})\frac{500}{300} \approx 3.3\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(d) Increase in internal energy M1·M1·A1

For a monatomic ideal gas $U = \tfrac{3}{2} n R T$, so $\Delta U = \tfrac{3}{2} n R \,\Delta T$ with $\Delta T = 200\ \mathrm{K}$. (M1)

$$ \Delta U = \tfrac{3}{2}(2.0)(8.31)(200). $$

(M1 for substitution)

$$ \Delta U \approx 5.0\times 10^{3}\ \mathrm{J}. $$

(A1)

(e) Mean kinetic energy per molecule A1·R1

Since $\bar{E}_k = \tfrac{3}{2} k_B T$, the mean kinetic energy is proportional to absolute temperature, so it increases. (R1)

It changes by the factor $T_2/T_1 = 500/300 = 5/3 \approx 1.7$. (A1)

Insight. This problem threads three sub-topics through one sample: $pV = nRT$ for the amount, $N = n N_A$ for the count, and $U = \tfrac{3}{2} n R T$ for the energy. The recurring shortcut is that every "per kelvin" quantity scales by the temperature ratio, so pressure, internal energy and mean kinetic energy all rise by $500/300$. Heating at constant volume does no work on the gas, so all the energy supplied goes into internal energy; that is why $\Delta U$ here is simply $\tfrac{3}{2} n R \,\Delta T$.

(a) 物质的量 M1·M1·A1

用 $pV = nRT$,故 $n = pV/(RT)$,其中 $T = 300\ \mathrm{K}$。(M1)

$$ n = \frac{(2.0\times 10^{5})(0.025)}{(8.31)(300)}. $$

(代入得 M1)

$$ n = \frac{5000}{2493} \approx 2.0\ \mathrm{mol}. $$

(A1)

(b) 分子数 M1·A1

$N = n N_A$:(M1)

$$ N = (2.0)(6.02\times 10^{23}) \approx 1.2\times 10^{24}. $$

(A1)

(c) 恒容下的新压强 M1·A1

体积恒定,故 $p \propto T$(盖-吕萨克):$p_2 = p_1 (T_2/T_1)$。(M1)

$$ p_2 = (2.0\times 10^{5})\frac{500}{300} \approx 3.3\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(d) 内能的增加 M1·M1·A1

单原子理想气体 $U = \tfrac{3}{2} n R T$,故 $\Delta U = \tfrac{3}{2} n R \,\Delta T$,其中 $\Delta T = 200\ \mathrm{K}$。(M1)

$$ \Delta U = \tfrac{3}{2}(2.0)(8.31)(200). $$

(代入得 M1)

$$ \Delta U \approx 5.0\times 10^{3}\ \mathrm{J}. $$

(A1)

(e) 每分子平均动能 A1·R1

因 $\bar{E}_k = \tfrac{3}{2} k_B T$,平均动能与绝对温度成正比,故增大。(R1)

它变为原来的 $T_2/T_1 = 500/300 = 5/3 \approx 1.7$ 倍。(A1)

要点。本题把三个子专题穿在同一样品上:$pV = nRT$ 求量,$N = n N_A$ 求数,$U = \tfrac{3}{2} n R T$ 求能。反复出现的捷径是每个"每开尔文"量都按温度比缩放,故压强、内能与平均动能都按 $500/300$ 增大。恒容加热不对气体做功,故所供能量全部转入内能;这正是此处 $\Delta U$ 恰为 $\tfrac{3}{2} n R \,\Delta T$ 的原因。
Q9HARDPaper 2combined gas law + real vs ideal合并气体定律与真实/理想气体[10 marks]

Fixed mass: $1.0\times 10^{5}\ \mathrm{Pa}$, $0.020\ \mathrm{m^{3}}$, $300\ \mathrm{K}$ to $0.010\ \mathrm{m^{3}}$, $350\ \mathrm{K}$. (a) combined gas law and its condition; (b) final pressure; (c) four ideal-gas assumptions and the two that fail near condensation; (d) conditions for ideal behaviour and why.固定质量:$1.0\times 10^{5}\ \mathrm{Pa}$、$0.020\ \mathrm{m^{3}}$、$300\ \mathrm{K}$ 变到 $0.010\ \mathrm{m^{3}}$、$350\ \mathrm{K}$。(a) 合并气体定律及其条件;(b) 末压强;(c) 四条理想假设及凝结附近失效的两条;(d) 理想行为的条件及原因。

Answers:答案:  (a) $p_1V_1/T_1 = p_2V_2/T_2$, fixed amount of gas  ·  (b) $p_2 \approx 2.3\times 10^{5}\ \mathrm{Pa}$  ·  (c) point molecules & no intermolecular forces fail  ·  (d) low pressure, high temperature

(a) Combined gas law and its condition A1·B1

For a fixed amount of gas the quantity $pV/T$ is constant: (A1)

$$ \frac{p_1 V_1}{T_1} = \frac{p_2 V_2}{T_2}. $$

It applies only when the amount of gas $n$ does not change between the two states (the cylinder is sealed). (B1)

(b) Final pressure M1·M1·A1

Rearrange for $p_2 = p_1 \dfrac{V_1}{V_2}\dfrac{T_2}{T_1}$, with all temperatures in kelvin. (M1)

$$ p_2 = (1.0\times 10^{5})\frac{0.020}{0.010}\cdot\frac{350}{300}. $$

(M1 for substitution)

$$ p_2 = (1.0\times 10^{5})(2.0)(1.1\overline{6}) \approx 2.3\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(c) Assumptions and the two that fail A1·A1·R1

An ideal gas assumes: molecules are point particles of negligible volume; there are no intermolecular forces except during collisions; collisions are perfectly elastic and motion is random; the collision time is negligible compared with the time between collisions. (A1·A1 for the four)

As the gas is strongly compressed and cooled towards condensation, the two that fail are the negligible-molecular-volume assumption (molecules are now crowded) and the no-intermolecular-forces assumption (slow molecules attract appreciably). (R1)

(d) Conditions for ideal behaviour A1·R1

A real gas behaves most ideally at low pressure and high temperature. (A1)

Low pressure keeps the molecules far apart so their own volume is negligible, and high temperature keeps them fast so intermolecular attractions are negligible: both assumptions then hold. (R1)

Insight. The combined gas law is just $pV = nRT$ with $nR$ cancelling between two states, which is exactly why "fixed amount of gas" is the stated condition; if the cylinder leaked, $n$ would change and the law would break. Handle the two ratios independently: halving the volume alone doubles the pressure, and the modest temperature rise nudges it up by a further $350/300$. Part (d) is the standard real-gas mark: always tie "low pressure" to molecular separation and "high temperature" to negligible attractions, never just assert the conditions.

(a) 合并气体定律及其条件 A1·B1

对固定气体量,$pV/T$ 为常数:(A1)

$$ \frac{p_1 V_1}{T_1} = \frac{p_2 V_2}{T_2}. $$

它仅当两态间气体量 $n$ 不变时适用(气缸密封)。(B1)

(b) 末压强 M1·M1·A1

解出 $p_2 = p_1 \dfrac{V_1}{V_2}\dfrac{T_2}{T_1}$,温度全用开尔文。(M1)

$$ p_2 = (1.0\times 10^{5})\frac{0.020}{0.010}\cdot\frac{350}{300}. $$

(代入得 M1)

$$ p_2 = (1.0\times 10^{5})(2.0)(1.1\overline{6}) \approx 2.3\times 10^{5}\ \mathrm{Pa}. $$

(A1)

(c) 假设及失效的两条 A1·A1·R1

理想气体假设:分子为体积可忽略的质点;除碰撞外无分子间作用力;碰撞完全弹性且运动随机;碰撞时间相对碰撞间隔可忽略。(四条得 A1·A1)

当气体被强烈压缩并冷却趋近凝结时,失效的两条是分子体积可忽略的假设(分子现已拥挤)与无分子间作用力的假设(慢分子间有明显吸引)。(R1)

(d) 理想行为的条件 A1·R1

真实气体在低压、高温下最接近理想。(A1)

低压使分子彼此远离故自身体积可忽略,高温使分子运动快故分子间吸引可忽略:两条假设便都成立。(R1)

要点。合并气体定律不过是 $pV = nRT$ 在两态间约去 $nR$,这正是"固定气体量"作为条件的原因;若气缸泄漏,$n$ 改变,定律便失效。把两个比值分开处理:仅体积减半就使压强翻倍,温度的小幅上升再按 $350/300$ 推高。(d) 是真实气体的标准得分点:务必把"低压"与分子间距、"高温"与吸引可忽略挂钩,切勿只陈述条件。
Q10HARDPaper 2HL ONLYkinetic theory: rms speed from $\bar{E}_k$动理论:由 $\bar{E}_k$ 求方均根速率[8 marks]

Helium ($M = 4.0\ \mathrm{g\,mol^{-1}}$) at $300\ \mathrm{K}$, monatomic ideal. (a) mass of one atom; (b) mean translational KE; (c) rms speed from $\tfrac{1}{2}m\overline{c^{2}} = \tfrac{3}{2}k_BT$; (d) compare rms speed of argon ($M = 40$) at the same $T$.氦($M = 4.0\ \mathrm{g\,mol^{-1}}$)于 $300\ \mathrm{K}$,单原子理想。(a) 单原子质量;(b) 平均平动动能;(c) 由 $\tfrac{1}{2}m\overline{c^{2}} = \tfrac{3}{2}k_BT$ 求方均根速率;(d) 比较同温下氩($M = 40$)的方均根速率。

Answers:答案:  (a) $m \approx 6.6\times 10^{-27}\ \mathrm{kg}$  ·  (b) $\bar{E}_k \approx 6.2\times 10^{-21}\ \mathrm{J}$  ·  (c) $c_{\mathrm{rms}} \approx 1.4\times 10^{3}\ \mathrm{m\,s^{-1}}$  ·  (d) argon slower, by factor $\sqrt{10}$

(a) Mass of one helium atom M1·A1

Convert the molar mass to $\mathrm{kg\,mol^{-1}}$ and divide by $N_A$: $m = M/N_A$. (M1)

$$ m = \frac{4.0\times 10^{-3}}{6.02\times 10^{23}} \approx 6.6\times 10^{-27}\ \mathrm{kg}. $$

(A1)

(b) Mean translational kinetic energy M1·A1

Use $\bar{E}_k = \tfrac{3}{2} k_B T$: (M1)

$$ \bar{E}_k = \tfrac{3}{2}(1.38\times 10^{-23})(300) \approx 6.2\times 10^{-21}\ \mathrm{J}. $$

(A1)

(c) Root-mean-square speed M1·A1

Set $\tfrac{1}{2} m \overline{c^{2}} = \bar{E}_k$, so $\overline{c^{2}} = 2\bar{E}_k/m$ and $c_{\mathrm{rms}} = \sqrt{\overline{c^{2}}}$. (M1)

$$ \overline{c^{2}} = \frac{2(6.21\times 10^{-21})}{6.64\times 10^{-27}} \approx 1.87\times 10^{6}\ \mathrm{m^{2}\,s^{-2}}, $$ $$ c_{\mathrm{rms}} = \sqrt{1.87\times 10^{6}} \approx 1.4\times 10^{3}\ \mathrm{m\,s^{-1}}. $$

(A1)

(d) Comparison with argon A1·R1

At the same temperature both gases have the same mean translational kinetic energy $\tfrac{3}{2} k_B T$, so $\tfrac{1}{2} m \overline{c^{2}}$ is the same for both. (R1)

Therefore $c_{\mathrm{rms}} \propto 1/\sqrt{m}$. Argon is $10$ times heavier, so its rms speed is smaller by a factor of $\sqrt{10} \approx 3.2$. (A1)

Insight. Equal temperature means equal kinetic energy, not equal speed; this is the most tested idea in B3.5. Because $\bar{E}_k = \tfrac{1}{2} m \overline{c^{2}}$ is fixed by $T$, the rms speed scales as $1/\sqrt{m}$, so the lighter gas is always faster. Watch two unit traps: the molar mass must be converted to $\mathrm{kg\,mol^{-1}}$ before dividing by $N_A$, and the rms speed is the square root of the mean-square speed, not the mean-square speed itself.

(a) 单个氦原子的质量 M1·A1

把摩尔质量换成 $\mathrm{kg\,mol^{-1}}$ 再除以 $N_A$:$m = M/N_A$。(M1)

$$ m = \frac{4.0\times 10^{-3}}{6.02\times 10^{23}} \approx 6.6\times 10^{-27}\ \mathrm{kg}. $$

(A1)

(b) 平均平动动能 M1·A1

用 $\bar{E}_k = \tfrac{3}{2} k_B T$:(M1)

$$ \bar{E}_k = \tfrac{3}{2}(1.38\times 10^{-23})(300) \approx 6.2\times 10^{-21}\ \mathrm{J}. $$

(A1)

(c) 方均根速率 M1·A1

令 $\tfrac{1}{2} m \overline{c^{2}} = \bar{E}_k$,故 $\overline{c^{2}} = 2\bar{E}_k/m$,$c_{\mathrm{rms}} = \sqrt{\overline{c^{2}}}$。(M1)

$$ \overline{c^{2}} = \frac{2(6.21\times 10^{-21})}{6.64\times 10^{-27}} \approx 1.87\times 10^{6}\ \mathrm{m^{2}\,s^{-2}}, $$ $$ c_{\mathrm{rms}} = \sqrt{1.87\times 10^{6}} \approx 1.4\times 10^{3}\ \mathrm{m\,s^{-1}}. $$

(A1)

(d) 与氩的比较 A1·R1

同温下两种气体平均平动动能相同,均为 $\tfrac{3}{2} k_B T$,故两者 $\tfrac{1}{2} m \overline{c^{2}}$ 相同。(R1)

因此 $c_{\mathrm{rms}} \propto 1/\sqrt{m}$。氩重 $10$ 倍,故其方均根速率小至 $1/\sqrt{10} \approx 1/3.2$。(A1)

要点。温度相同意味着动能相同,而非速率相同;这是 B3.5 最常考的观念。因 $\bar{E}_k = \tfrac{1}{2} m \overline{c^{2}}$ 由 $T$ 固定,方均根速率按 $1/\sqrt{m}$ 缩放,故更轻的气体总是更快。注意两个单位陷阱:除以 $N_A$ 前须把摩尔质量换成 $\mathrm{kg\,mol^{-1}}$,且方均根速率是均方速率的平方根,而非均方速率本身。