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Molarity
Preparing a solution
Dilution
Solubility rules
Complete & Net Ionic Equations
Colligative properties
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Heat Flow
Energy diagrams
Thermochemical equations
Heating/ Cooling curves
Specific Heat Capacity
Calorimetry
Hess's Law
Enthalpies of formation
Bond enthalpies
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Collision Theory
Rate Comparisons
Integrated Rate Law
Differential Rate Law
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Equilibrium
Equilibrium Expression
ICE Tables
Calculating K
K vs Q
Le Chatelier's Principle
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Definitions
Conjugate Acids & Base Pairs
Autoionization of water
pH Scale
Strong Acids/ Bases
Ka and Kb
Buffer
Titrations
Indicators
pH salts
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Entropy
Gibb's Free Energy
G and Temperature
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Oxidation numbers
Half Reactions
Balancing Redox reactions
Voltaic cells
Cell potential (standard conditions)
Cell potential (non-standard)
Electrolysis
Quantitative Electrochemistry
UV-VIS Spectroscopy
Related Examples and Practice Problems
Additional Worked Out Examples/ Practice
Identifying classification types: Differentiation between elements, compounds or mixtures and homogeneous and heterogenous mixtures
Separation techniques: Selected and explaining limitation of appropriate separation
Relating Properties to Composition: Predicting classification based on descriptive properties
and more …
Topic Summary & Highlights
and Help Videos
Core Concept
UV-Vis spectroscopy doesn't directly measure the light a molecule absorbs. Instead, it measures the light that gets transmitted through the sample. The key parameter is absorbance (A), which is related to the amount of light absorbed by the sample and the concentration of the absorbing molecule.
Higher absorbance: Indicates a greater portion of light is absorbed, suggesting a strong interaction between the light and the molecule.
Lower absorbance: Indicates less light is absorbed, possibly because the light doesn't have the right energy to excite the molecule.
Interpreting the Spectrum
The results of a UV-Vis experiment are presented as an absorption spectrum, a graph of absorbance versus wavelength of light. This spectrum is like a fingerprint of the molecule, providing valuable information:
λmax (lambda max): The wavelength at which the molecule exhibits maximum absorbance. This value can be linked to the type of electronic transitions occurring within the molecule.
Functional Groups: Different functional groups (e.g., C=C double bonds, carbonyl groups) tend to absorb light at specific wavelength ranges. Analyzing the λmax can help identify these functional groups within the molecule.
Applications of UV-Vis Spectroscopy:
Identifying Unknown Molecules: By comparing the absorption spectrum of an unknown molecule to a library of known spectra, chemists can potentially identify its structure.
Monitoring Chemical Reactions: As a reaction progresses, the concentration of reactants and products might change. UV-Vis spectroscopy can be used to track these changes by monitoring the absorbance at specific wavelengths.
Quantifying Analytes: The relationship between absorbance and concentration can be used to determine the amount of a specific molecule present in a solution.
The Beer-Lambert Law: A Powerful Duo
While Beer's Law is often used independently, it's actually part of a broader principle called the Beer-Lambert Law. This law states that the absorbance (A) of light by a solution is directly proportional to the:
Concentration (c): The higher the concentration of the colored molecule, the more light particles (photons) it has a chance to absorb, leading to higher absorbance.
Path Length (l): This is the length of the light's travel path through the solution. A longer path allows for more interaction between light and molecules, potentially leading to greater absorbance.
The Equation Unveiling the Mystery:
The Beer-Lambert Law is expressed by the following equation:
A = ε • l • c
A: Absorbance (unitless)
ε (epsilon): Molar Absorptivity Coefficient (a constant specific to the colored molecule and wavelength of light, with units of L mol^-1 cm^-1)
l: Path Length (usually the width of the cuvette holding the solution, in cm)
c: Concentration of the colored molecule (usually in Molarity, mol/L)
Applications of Beer's Law:
Quantifying Unknown Concentrations: If we know the molar absorptivity coefficient (ε) and path length (l) for a specific colored molecule at a particular wavelength, we can measure the absorbance (A) of a solution and use Beer's Law to calculate the unknown concentration (c) of that molecule.
Monitoring Chemical Reactions: As a reaction progresses, the concentration of the colored reactant or product might change. By monitoring the absorbance at a specific wavelength using Beer's Law, we can track the reaction's progress.
Calibrating Spectrophotometers: These instruments measure absorbance. Beer's Law allows us to use solutions with known concentrations to create a calibration curve, relating absorbance to concentration for a specific molecule and wavelength.
Tips for Studying UV-Vis Spectroscopy:
Understand the relationship between wavelength, energy, and electronic transitions.
Practice interpreting absorption spectra, identifying λmax and relating it to potential electronic transitions.
Learn how UV-Vis spectroscopy can be used to identify functional groups and for quantitative analysis.
Explore online simulations and resources that visualize light-matter interactions in UV-Vis spectroscopy.