hs: fix katex
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@ -343,15 +343,19 @@ When a solution is **diluted** the moles of solute are the same before and after
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$$c_iv_i=c_fv_f$$
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A mass/mass percentage concentration (%m/m) is such that:
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$$c\text{ (%m/m)}=\frac{\text{mass of solute (g)}}{\text{total mass of solution (g)}}×100\%$$
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A mass/volume percentage concentration (%m/v) is easy to measure, but may be unreliable as volume changes with temperature. It is such that:
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$$c\text{ (%m/v)}=\frac{\text{mass of solute (g)}}{\text{total volume of solution (100 cm}^3\text{)}}×100\%$$
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A volume/volume percentage concentration (%v/v) has the same properties as the above but also has the caveat that there is no guarantee that the total volume of the solution is equal to the sums of the volumes of the solute and solvent. It is such that:
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$$c\text{ (%v/v)}=\frac{\text{volume of solute (cm}^3\text{)}}{\text{total volume of solution (100 cm}^3\text{)}}×100\%$$
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When dealing with very small concentrations, smaller units such as **parts per million (ppm)** or parts per billion (ppb) are used.
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$$c\text{ (ppm)}=\frac{\text{mass of solute (g)}}{\text{mass of solution (g)}}×10^6$$
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### Standard solutions
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@ -465,8 +469,10 @@ Isotopes are atoms of the same element but with different masses, or alternative
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The mass of every atom is represented relative to 1/12th of a carbon-12 atom. This mass is either unitless or expressed in terms of **atomic mass units (amu or u)**. On the periodic table, the **relative atomic mass** ($A_r$) is shown, which is the sum of the masses of each isotope combined with their natural abundance (%abundance).
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$$A_r = \text{%abundance}×\text{mass number of isotope}$$
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$$m_a = \Sigma A_r$$
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$$
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A_r = \text{%abundance}×\text{mass number of isotope} \\
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m_a = \Sigma A_r
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$$
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When calculating the atomic mass from the graph from a **mass spectrometer**, the sum of the natural abundances of each isotope may not equal 100 or 1 (not in %abundance). In this case, calculation of %abundance will need to be done before solving for $m_a$.
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@ -1024,7 +1024,7 @@ Circular motion is any motion along a circular path. The instantaneous velocity
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!!! definition
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- An object is in **uniform circular motion** when all instantaneous velocities are equal in magnitude or when all accelerations are equal in magnitude.
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- **Period** ($T$) represents the time required to complete one revolution ($360°$ or $2\pi$ radians).
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- **Frequency** ($f$) represents the revolutions per second represented in hertz ($\text{1 Hz=1s^{-1}}$), and is the inverse of period.
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- **Frequency** ($f$) represents the revolutions per second represented in hertz ($\text{1 Hz=1 s}^{-1}$), and is the inverse of period.
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!!! warning
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As velocity and acceleration are vectors, direction must be considered when manipulating them. This means that the **kinematic equations** cannot be used.
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@ -712,7 +712,8 @@ $$\ce{14 = pH + pOH}$$
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### Acid/base dissociation
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An equilibrium will be reached when a weak acid or base dissociates/ionises in water. The extent that the acid or base has dissociated/ionised can be quantified with **percent dissociation/ionisation**.
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$$\text{% ionisation} = \frac{\text{[acid ionised]}}{\text{[original acid]}}\times 100\%$$
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$$\text{\% ionisation} = \frac{\text{[acid ionised]}}{\text{[original acid]}}\times 100\%$$
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!!! note
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When performing an approximation assumption in an ICE table, the assumption is also valid if the % ionisation is less than 5%.
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