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Vocabulary practice flashcards covering basic principles of acids, bases, salts, and foundations of organic chemistry including functional groups and hybridization.
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Arrhenius acid
A hydrogen-containing compound that produces H+ ions in solution (adding water).
Arrhenius base
A hydroxide-containing compound that produces OH− (Hydroxide) ions in solution.
Ionization
The process in which individual positive and negative ions are produced from a molecular compound that is dissolved in solution (in water).
Dissociation
The process in which individual positive and negative ions are released from an ionic compound that is dissolved in solution.
Bronsted-Lowry Acid
A substance that can donate a proton (H+ ion) to some other substance; a proton donor.
Bronsted-Lowry Base
A substance that can accept a proton (H+ ion) from some other substance; a proton acceptor.
Conjugate Acid
The species that is formed when a base accepts a proton.
Conjugate Base
The product that is left behind (ion left) after an acid has donated its proton.
Acid Ionization Equilibrium
The state at which the rate of the forward reaction between acids and bases is equal to the rate of the product formation.
Amphiprotic Substance
A substance that can either lose or accept a proton and thus can function as either a Bronsted-Lowry Acid or a Bronsted-Lowry base, such as H2O.
Monoprotic Acid
An acid that supplies one proton (H+ ion) per molecule during an acid-base reaction.
Diprotic Acid
An acid that supplies two protons (H+ ions) per molecule during an acid-base reaction.
Polyprotic Acid
An acid that supplies two or more protons (H+ ions) during an acid-base reaction, including both diprotic and triprotic acids.
Strong Acid
An acid that transfers approximately 100% of its protons to water in an aqueous solution; its ionization equilibrium lies far to the right.
Acid Ionization Constant (Ka)
The equilibrium constant for the reaction of a weak acid with water where Ka=[HA][H3O+][A−].
Neutralization Reaction
The chemical reaction between an acid and a hydroxide base in which a salt and water are the products.
Self-ionization of Water
A process where water molecules in pure water interact with one another to form equal amounts of hydronium and hydroxide ions: H2O+H2O⇌H3O++OH−.
Ion Production Constant for Water (Kw)
At 24∘C, the product of the concentrations of hydronium and hydroxide ions, which must always equal 1.00×10−14.
pH for a solution with whole number concentration
Calculated by pH=−log[H+]; for example, if [H+]=1×10−5, the pH is 5.
Buffer
An aqueous solution containing substances that prevent major changes in solution pH when small amounts of acid or base are added to it.
Henderson-Hasselbalch Equation
An equation used to calculate the pH of a buffer: pH=pKa+log[HA][A−].
Organic Chemistry
The study of the compounds of carbon.
Structural Formula
A representation that shows the atoms in a molecule and the bonds that connect them.
Electronegativity (EN)
The intrinsic ability of an atom to attract the shared electrons in a covalent bond.
Addition Reaction
An organic reaction where two molecules combine to form a single product.
Elimination Reaction
An organic reaction where one molecule splits into two products.
Substitution Reaction
An organic reaction where parts from two molecules exchange with each other.
Hybridization
The mixing of different orbitals of a single atom to produce an equal number of hybrid orbitals of the same energy and identical properties.
Sigma (σ) Bond
A bond formed by the overlap of two hybrid orbitals through areas of maximum electron density at the tips of the lobes.
Pi (π) Bond
A bond formed by the overlap of two unhybridized, parallel p orbitals at the sides of the lobes.
sp3 Hybridization
Also called tetrahedral hybridization; involves combining one s orbital and three p orbitals to form four hybrid orbitals at angles of 109.5∘.
sp2 Hybridization
Also called trigonal hybridization; involves combining one s orbital and two p orbitals to produce three orbitals directed toward the corners of an equilateral triangle at 120∘.
sp Hybridization
Also known as diagonal hybridization; involves combining one s orbital and one p orbital at an angle of 180∘.
Functional Group
An atom or group of atoms within a molecule that has similar chemical properties whenever it appears in various compounds.
Alkane
A hydrocarbon containing only carbon-carbon single bonds with the general formula CnH2n+2.
Constitutional Isomers
Compounds that have the same molecular formula but different structural formulas (different connectivity).
Cycloalkane
A cyclic hydrocarbon in which all carbons of the ring are saturated.
Alcohols
Compounds containing an −OH (hydroxyl) group bonded to a tetrahedral carbon atom.
Thiol
A compound containing an −SH (sulfhydryl) group, often associated with strong, unpleasant odors.
Carbonyl Group
A functional group common to aldehydes and ketones, consisting of a carbon-oxygen double bond (C=O).
Fischer Esterification
The reaction of a carboxylic acid with an alcohol in the presence of an acid catalyst to prepare an ester.
Saponification
The hydrolysis of an ester using a hot aqueous base to produce a carboxylic acid salt and an alcohol.
Aliphatic Amine
An amine in which all carbons bonded to nitrogen are derived from alkyl groups.
Kevlar
A polyaromatic amide (polyamide) made from an aromatic dicarboxylic acid and an aromatic diamine.