AP®︎ Chemistry: Unit 1 Flashcards

Master key terms and definitions for Unit 1 of AP Chemistry – Atomic Structure and Properties to help you prep for quizzes and the AP exam.


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Term

Molar Mass

Definition

The mass of one mole of a substance, usually expressed in g/mol.

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Molar Mass
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The mass of one mole of a substance, usually expressed in g/mol.

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Calculating Molar Mass
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Add each element's atomic mass multiplied by its subscript in the chemical formula.

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Moles-Mass Equation
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n = m/M, where m is mass in grams and M is molar mass.

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Subscripts and Particle Ratios
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Subscripts show atom ratios in a formula and determine particle-to-atom conversion relationships.

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Mole and Avogadro's Number
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One mole contains 6.022 × 10^23 representative particles of a substance.

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Atomic Mass and Molar Mass Relationship
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A particle's average mass in amu equals that substance's molar mass numerically in g/mol.

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Dimensional Analysis
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A conversion method using molar mass or Avogadro's number so units cancel correctly.

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Isotopes
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Atoms of the same element with different numbers of neutrons and different masses.

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Peak Position and Peak Height in a Mass Spectrum
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Peak position gives isotope mass; peak height or area gives relative abundance.

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Relative Abundance
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The proportion of each isotope in nature, usually written as a percent or decimal.

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Abundances Sum to 100%
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All isotope percentages for one element must add to 100%, or 1.00 as decimals.

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Estimating the Most Abundant Isotope from Average Atomic Mass
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The average lies closest to the isotope with the greatest natural abundance.

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Identifying an Element from Its Mass Spectrum
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Match the spectrum’s isotope masses and weighted average to the element’s periodic-table atomic mass.

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Mass Spectrum of an Element
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A graph from mass spectrometry showing isotope masses and relative abundances for one element.

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Average Atomic Mass
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The weighted average of isotope masses calculated using each isotope’s natural abundance.

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Isotope Mass
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The mass of a specific isotope, approximately equal to its protons plus neutrons.

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Pure Substance
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Matter with a constant composition made of only one kind of particle.

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Elements and Compounds
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Elements contain one type of atom; compounds contain two or more elements chemically combined.

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Molecule vs. Formula Unit
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Molecules are discrete covalent particles; formula units are lowest whole-number ratios in ionic compounds.

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Law of Definite Proportions / Law of Constant Composition
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A pure compound always contains the same elements in the same mass ratio.

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Empirical Formula
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The lowest whole-number ratio of atoms of each element in a compound.

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Empirical Formula from Percent Composition
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Assume 100 g, convert each element to moles, divide by the smallest, then multiply to whole numbers.

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Formula Unit
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The lowest whole-number ratio of ions used to represent an ionic compound; counted as the representative particle for ionic substances.

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Percent Composition By Mass
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The percent of a compound's total mass contributed by each element, found by dividing the mass of each element by the total mass and multiplying by 100%.

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Pure Substance vs. Mixture
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A pure substance has one type of particle; a mixture has two or more in variable proportions.

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Homogeneous vs. Heterogeneous Mixtures
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Homogeneous mixtures are uniform throughout; heterogeneous mixtures have visibly nonuniform composition.

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Particle Diagrams of Mixtures
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Use counts and types of particles shown to determine composition, relative amounts, and whether a sample is pure.

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Distillation
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Separates liquid mixture components by differences in boiling point through vaporization and condensation.

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Filtration
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Separates insoluble solids from liquids using a porous barrier that traps larger particles.

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Thin-Layer Chromatography
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Separates mixture components by different attractions to a stationary phase and a mobile solvent.

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Stationary Phase vs. Mobile Phase
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The stationary phase stays fixed; the mobile phase moves and carries substances past it.

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Polarity in Thin-Layer Chromatography
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More polar substances stick more to polar silica, while less polar substances travel farther with nonpolar solvent.

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Retention Factor (Rf)
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The distance traveled by a component divided by the distance traveled by the solvent front.

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Elemental Analysis and Empirical Formula
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Uses element masses or percentages to find simplest whole-number atom ratios and assess purity.

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Coulomb's Law
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Electrostatic force is proportional to charge product and inversely proportional to distance squared.

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Shells, Subshells, Core Electrons, and Valence Electrons
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Shells are energy levels; subshells are s, p, d, f; inner electrons are core, outer are valence.

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Subshells
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s holds 2 electrons, p 6, d 10, and f 14.

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Aufbau Principle
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Electrons fill the lowest-energy orbitals available before occupying higher-energy orbitals.

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Pauli Exclusion Principle
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An orbital can hold at most two electrons, and they must have opposite spins.

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Hund's Rule
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Electrons occupy equal-energy orbitals singly before any pairing occurs.

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Ground-State Electron Configuration
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The lowest-energy arrangement of an atom's or ion's electrons among orbitals.

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Noble Gas Shortcut
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Use the previous noble gas in brackets, then write only the remaining outer subshells.

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Orbital Diagram
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A box-and-arrow model showing orbital occupancy and electron spins in each subshell.

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Electron Configuration of Ions
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Add electrons for anions and remove highest-energy outer electrons for cations.

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Subatomic Particles
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Atoms contain protons and neutrons in the nucleus and electrons outside it.

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Photoelectron Spectroscopy (PES)
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A technique that measures electron binding energies by ejecting electrons with high-energy photons.

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Binding Energy
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The energy required to remove an electron from an atom, ion, or subshell.

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Ground-State Electron Configuration from PES
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Assign peaks to subshells by binding energy and use peak sizes to count electrons.

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Photoelectric Effect and PES
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Photons eject electrons only if they provide enough energy to overcome the electrons' binding energies.

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Interpreting a Photoelectron Spectrum
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A graph where each subshell forms a peak whose position shows binding energy and height shows electron count.

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Electron-Nucleus Attraction in PES
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Electrons closer to the nucleus have higher binding energies than valence electrons because attraction is stronger.

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Periodicity
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Recurring patterns in element properties caused by repeating valence electron configurations.

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Periods and Groups
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Periods are rows with the same occupied shells; groups are columns with similar valence electrons.

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Valence Electrons and Group Properties
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Elements in the same group have similar outer electrons and therefore similar chemical behavior.

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Shell Model
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Electrons occupy energy levels around the nucleus, with outer levels farther away and more shielded.

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Coulomb's Law in Periodic Trends
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Electrostatic attraction increases with greater charge and decreases as distance between charges increases.

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Atomic Radius Trend
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Decreases across a period and increases down a group because of charge and shell effects.

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Ionic Radius
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Cations are smaller than their atoms; anions are larger than their atoms.

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Using Ionization Energies to Find Valence Electrons
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Identify the large jump in values; electrons removed before it are the valence electrons.

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Periodic Trend Predictions
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Use an element's position, shells, shielding, and effective nuclear charge to estimate atomic properties.

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Electron Affinity
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Energy change when a gaseous atom gains an electron, generally more negative across periods and down groups less negative.

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Effective Nuclear Charge And Shielding
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Inner electrons shield outer electrons from the full nuclear charge, so an electron experiences a reduced net positive attraction called effective nuclear charge.

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Ionization Energy
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The energy required to remove an electron from an atom; it increases with stronger nucleus-electron attraction, generally increasing across a period and decreasing down a group.

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Valence Electrons From Periodic Table Position
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For main-group elements, the group number gives the number of outermost electrons.

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Analogous Compounds
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Elements in the same group form similar compounds because they have the same valence electron pattern.

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Typical Ionic Charges by Group
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Group 1: +1, Group 2: +2, Group 13: +3, Group 15: -3, Group 16: -2, Group 17: -1.

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Ionic Bond
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Electrostatic attraction between oppositely charged ions formed after electron transfer.

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Ionic Compound Formula Prediction
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Combine ions in the smallest whole-number ratio that makes the total charge zero.

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Ions, Cations, and Anions
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Charged atoms or molecules are positive after electron loss and negative after electron gain.

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Octet Rule and Noble Gas Configuration
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Main-group atoms often gain or lose electrons to achieve a stable noble-gas-like valence shell.

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Valence Electrons
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The outermost electrons, usually in the highest principal energy level for main-group elements, that are involved in bonding; they can be identified from electron configuration by counting the outer s and p electrons.

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Electronegativity
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An atom's ability to attract shared electrons in a bond; it generally increases across a period and decreases down a group and helps predict whether atoms gain, lose, or share electrons.

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Ionization Energy Gap And Valence Electrons
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In successive ionization energies, each electron removed requires more energy, and a large jump after several removals indicates that all valence electrons have been removed; the number removed before the jump equals the number of valence electrons.

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