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Flashcards on predicting reaction direction, acid-base strength, and Lewis acids/bases.
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The side of a reaction that the equilibrium will favor, characterized by weaker acids and bases.
Conjugate Acid
The acid formed when a base accepts a proton.
Conjugate Base
The remaining substance after an acid donates a proton.
Bronsted-Lowry Acid
Species that donates a proton.
Bronsted-Lowry Base
Species that accepts a proton.
Curved Arrows
A method to visually represent the movement of electrons in a reaction mechanism.
Lewis Acid
Species that accepts an electron pair.
Lewis Base
Species that donates an electron pair.
Electrophile
Another term for something that would like to have pairs of electrons, meaning it has an available orbital to accept an electron pair
Nucleophile
Seeking out a nucleus to donate its electron pair onto.
Alkane
A hydrocarbon containing only single bonds between carbon atoms.
Aliphatic Hypercarbons
Acyclic hydrocarbons that only contain carbon and hydrogen single bonds.
Aromatic Hypercarbons
Hydrocarbons containing alternating arrays of double and single bonds in a ring.
Hydrocarbon
A compound containing only carbon and hydrogen atoms
Covalent Bonds
A shared pair of electrons, where one electron comes from each atom in the bond.
Sigma Bond
Overlapping in an end on end arrangement as the most direct way to hold atoms together.
SP3 Hybridized
The carbon atoms are tetrahedral
Sigma bond
It relies on end on end or overlap as the most direct way to hold atoms together.
Alkene
A double bond is made up of a single bond and a pi bond
A triple bond is made up of a single bond and two pi bonds
Alkyne
Pi bond is weaker than sigma bond.
Because the orbitals are only overlapping side to side and not end on end.