Organic Biochemistry Lecture Notes

0.0(0)
Studied by 0 people
call kaiCall Kai
Locked
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
GameKnowt Play
Card Sorting

1/43

flashcard set

Earn XP

Description and Tags

Vocabulary practice flashcards covering basic principles of acids, bases, salts, and foundations of organic chemistry including functional groups and hybridization.

Last updated 5:56 AM on 7/30/26
Name
Mastery
Learn
Test
Matching
Spaced
Call with Kai
Chat

No analytics yet

Send a link to your students to track their progress

44 Terms

1
New cards

Arrhenius acid

A hydrogen-containing compound that produces H+H^+ ions in solution (adding water).

2
New cards

Arrhenius base

A hydroxide-containing compound that produces OHOH^- (Hydroxide) ions in solution.

3
New cards

Ionization

The process in which individual positive and negative ions are produced from a molecular compound that is dissolved in solution (in water).

4
New cards

Dissociation

The process in which individual positive and negative ions are released from an ionic compound that is dissolved in solution.

5
New cards

Bronsted-Lowry Acid

A substance that can donate a proton (H+H^+ ion) to some other substance; a proton donor.

6
New cards

Bronsted-Lowry Base

A substance that can accept a proton (H+H^+ ion) from some other substance; a proton acceptor.

7
New cards

Conjugate Acid

The species that is formed when a base accepts a proton.

8
New cards

Conjugate Base

The product that is left behind (ion left) after an acid has donated its proton.

9
New cards

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.

10
New cards

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 H2OH_2O.

11
New cards

Monoprotic Acid

An acid that supplies one proton (H+H^+ ion) per molecule during an acid-base reaction.

12
New cards

Diprotic Acid

An acid that supplies two protons (H+H^+ ions) per molecule during an acid-base reaction.

13
New cards

Polyprotic Acid

An acid that supplies two or more protons (H+H^+ ions) during an acid-base reaction, including both diprotic and triprotic acids.

14
New cards

Strong Acid

An acid that transfers approximately 100%100 \text{\%} of its protons to water in an aqueous solution; its ionization equilibrium lies far to the right.

15
New cards

Acid Ionization Constant (KaK_a)

The equilibrium constant for the reaction of a weak acid with water where Ka=[H3O+][A][HA]K_a = \frac{[H_3O^+][A^-]}{[HA]}.

16
New cards

Neutralization Reaction

The chemical reaction between an acid and a hydroxide base in which a salt and water are the products.

17
New cards

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+H2OH3O++OHH_2O + H_2O \rightleftharpoons H_3O^+ + OH^-.

18
New cards

Ion Production Constant for Water (KwK_w)

At 24C24\,^\circ\text{C}, the product of the concentrations of hydronium and hydroxide ions, which must always equal 1.00×10141.00 \times 10^{-14}.

19
New cards

pH for a solution with whole number concentration

Calculated by pH=log[H+]pH = -\log [H^+]; for example, if [H+]=1×105[H^+] = 1 \times 10^{-5}, the pH is 55.

20
New cards

Buffer

An aqueous solution containing substances that prevent major changes in solution pH when small amounts of acid or base are added to it.

21
New cards

Henderson-Hasselbalch Equation

An equation used to calculate the pH of a buffer: pH=pKa+log[A][HA]pH = pK_a + \log \frac{[A^-]}{[HA]}.

22
New cards

Organic Chemistry

The study of the compounds of carbon.

23
New cards

Structural Formula

A representation that shows the atoms in a molecule and the bonds that connect them.

24
New cards

Electronegativity (EN)

The intrinsic ability of an atom to attract the shared electrons in a covalent bond.

25
New cards

Addition Reaction

An organic reaction where two molecules combine to form a single product.

26
New cards

Elimination Reaction

An organic reaction where one molecule splits into two products.

27
New cards

Substitution Reaction

An organic reaction where parts from two molecules exchange with each other.

28
New cards

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.

29
New cards

Sigma (σ\sigma) Bond

A bond formed by the overlap of two hybrid orbitals through areas of maximum electron density at the tips of the lobes.

30
New cards

Pi (π\pi) Bond

A bond formed by the overlap of two unhybridized, parallel p orbitals at the sides of the lobes.

31
New cards

sp3 Hybridization

Also called tetrahedral hybridization; involves combining one s orbital and three p orbitals to form four hybrid orbitals at angles of 109.5109.5^\circ.

32
New cards

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 120120^\circ.

33
New cards

sp Hybridization

Also known as diagonal hybridization; involves combining one s orbital and one p orbital at an angle of 180180^\circ.

34
New cards

Functional Group

An atom or group of atoms within a molecule that has similar chemical properties whenever it appears in various compounds.

35
New cards

Alkane

A hydrocarbon containing only carbon-carbon single bonds with the general formula CnH2n+2C_nH_{2n+2}.

36
New cards

Constitutional Isomers

Compounds that have the same molecular formula but different structural formulas (different connectivity).

37
New cards

Cycloalkane

A cyclic hydrocarbon in which all carbons of the ring are saturated.

38
New cards

Alcohols

Compounds containing an OH-OH (hydroxyl) group bonded to a tetrahedral carbon atom.

39
New cards

Thiol

A compound containing an SH-SH (sulfhydryl) group, often associated with strong, unpleasant odors.

40
New cards

Carbonyl Group

A functional group common to aldehydes and ketones, consisting of a carbon-oxygen double bond (C=OC=O).

41
New cards

Fischer Esterification

The reaction of a carboxylic acid with an alcohol in the presence of an acid catalyst to prepare an ester.

42
New cards

Saponification

The hydrolysis of an ester using a hot aqueous base to produce a carboxylic acid salt and an alcohol.

43
New cards

Aliphatic Amine

An amine in which all carbons bonded to nitrogen are derived from alkyl groups.

44
New cards

Kevlar

A polyaromatic amide (polyamide) made from an aromatic dicarboxylic acid and an aromatic diamine.