Property | Acids | Bases |
---|---|---|
Taste | Sour | Bitter |
Feel | Corrosive | Slippery |
pH Range | 0–6.9 | 7.1–14 |
Ion Produced | H⁺ (hydrogen ions) | OH⁻ (hydroxide ions) |
Litmus Test | Turns red | Turns blue |
Conductivity | Good (if strong) | Good (if strong) |
Arrhenius Definition:
Acid: Increases H⁺ in water.
Base: Increases OH⁻ in water.
Brønsted-Lowry Definition:
Acid: Proton (H⁺) donor.
Base: Proton (H⁺) acceptor.
Strong: Fully ionize in water (e.g., HCl, NaOH).
Weak: Partially ionize (e.g., CH₃COOH, NH₃).
Scale from 0 to 14:
0–6 = acidic, 7 = neutral, 8–14 = basic
pH = -log[H⁺]
A change in 1 pH unit = 10× difference in [H⁺]
Acid + Base → Salt + Water
Example: HCl + NaOH → NaCl + H₂O
Used to find the concentration of an unknown acid or base using a known one.
Steps:
Add acid to base (or vice versa) using a burette.
Use an indicator (e.g., phenolphthalein).
Calculate unknown concentration using:
n = C × V (mol = concentration × volume)
C = n ÷ V
Complete Combustion: Fuel + O₂ → CO₂ + H₂O
Clean burn, efficient energy
Incomplete Combustion: Fuel + limited O₂ → CO + C (soot) + H₂O
Produces carbon monoxide, a toxic gas
Sulfur Dioxide (SO₂) from coal burning:
SO₂ + H₂O → H₂SO₃ (sulfurous acid)
SO₃ + H₂O → H₂SO₄ (sulfuric acid)
Nitrogen Oxides (NO, NO₂) from engines:
NO₂ + H₂O → HNO₃ (nitric acid)
These acids fall as acid rain, harming:
Aquatic life (lowers lake pH)
Plants (damages leaves, leaches nutrients)
Infrastructure (corrodes buildings/statues)
Human health (respiratory issues)
Limestone (CaCO₃): Natural base that neutralizes acids in soil and water.
Scrubbers: Remove SO₂ from smokestacks using limestone slurries.
Catalytic Converters: Reduce NO and CO in car exhaust by converting them to N₂ and CO₂.
Sunlight + NO₂ → NO + O
O + O₂ → O₃ (ozone, part of photochemical smog)
Effects: Eye irritation, breathing problems, damage to crops.
ppm (parts per million): 1 mg/L
ppb (parts per billion): 1 μg/L
The study of carbon-based compounds, especially hydrocarbons and their derivatives.
Compounds made of only carbon and hydrogen.
Type | Bonds | Ending | Example |
---|---|---|---|
Alkanes | Single | -ane | Methane (CH₄) |
Alkenes | Double | -ene | Ethene (C₂H₄) |
Alkynes | Triple | -yne | Ethyne (C₂H₂) |
Aromatics | Ring structures | varies | Benzene (C₆H₆) |
Groups of atoms that give molecules specific chemical properties and uses.
Group | Structure | Suffix | Properties / Functions / Uses |
---|---|---|---|
Alcohol | -OH | -ol | Polar, dissolves in water; used in disinfectants, fuels, drinking alcohol (ethanol). |
Carboxylic Acid | -COOH | -oic acid | Acidic, sour taste; found in vinegar (acetic acid), preservatives, and sour candies. |
Ester | -COO- | -oate | Sweet/fruity smell; used in perfumes, flavorings, solvents. |
Halide | -X (F, Cl, Br, I) | varies | Often non-polar; used in refrigerants, anesthetics, and pesticides. |
Ketone | C=O (internal) | -one | Solvent use (e.g., acetone), present in sugars. |
Aldehyde | -CHO | -al | Strong smells; used in perfumes, preservatives. |
Amine | -NH₂ | -amine | Basic; found in amino acids, drugs, dyes. |
Find the longest carbon chain with the functional group.
Number the chain from the end closest to the functional group.
Name branches (methyl, ethyl, etc.).
Use correct suffix based on the functional group.
For esters: name alcohol part first, acid part second.
Butanoic acid: 4 carbon acid
2-butanol: 4 carbon chain with OH on 2nd carbon
Ethyl ethanoate: Ester made from ethanol + ethanoic acid
Alcohol + Carboxylic Acid → Ester + Water
Example:
Ethanol + Propanoic Acid → Ethyl Propanoate + H₂O
Each carbon makes 4 bonds
Hydrogen makes 1 bond
Oxygen makes 2 bonds
Nitrogen makes 3 bonds
Acids donate H⁺, bases accept H⁺
Acid rain comes from burning fossil fuels
Esters = fruity smell (think “Ester = Easter = candy”)
Alcohol = OH = “Oh hi!” (disinfectants, drinking)
Carboxylic acid = sour (think vinegar or lemon)