3. Introduction to Organic Molecules and Functional Groups Flashcards

1
Q

An atom or group of atoms with characteristic chemical and physical properties. The functional group is the reactive part of the molecule.

A

Functional group

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2
Q

Atoms other than Carbon or Hydrogen. Commonly Nitrogen, Oxygen, Sulfur, Phosphorus, and Halogens

A

Heteroatoms

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3
Q

covalent chemical bonds, in each of which two lobes of an orbital on one atom overlap with two lobes of an orbital on another atom, and in which this overlap occurs laterally.

A

π Bonds

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4
Q

The C─C and C─H σ bond framework makes up the skeleton of an organic molecule.

A

Carbon backbone (Skeleton)

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5
Q

An alipathic hydrocarbon having only C-C and C-H σ bonds.

A

Alkane

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6
Q

An aliphatic hydrocarbon that contains a C-C double bond.

A

Alkene

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7
Q

An aliphatic hydrocarbon that contains a C-C triple bond.

A

Alkyne

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8
Q

A carbon atom that is bonded to one other carbon atom. May contain Primary Hydrogen (1° H)

A

Primary (1°) carbon

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9
Q

A carbon atom that is bonded to two other carbon atoms. May contain a Secondary Hydrogen (2° H)

A

Secondary (2°) carbon

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10
Q

A carbon atom that is bonded to three other carbon atoms. May contain a Tertiary Hydrogen (3° H)

A

Tertiary (3°) carbon

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11
Q

A carbon atom that is bonded to four other carbon atoms.

A

Quaternary (4°) carbon

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12
Q

An alcohol having the general structure RCH2OH.

A

Primary (1°) alcohol

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13
Q

An alcohol having the general structure R2CHOH.

A

Secondary (2°) alcohol

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14
Q

An alcohol having the general structure R3COH.

A

Tertiary (3°) alcohol

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15
Q

An amine having the general structure RNH2.

A

Primary (1°) amine

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16
Q

An amine having the general structure R2NH.

A

Secondary (2°) amine

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17
Q

An amine having the general structure R3N.

A

Tertiary (3°) amine

18
Q

A functional group that contains a carbon–oxygen double bond (C═O). The polar carbon–oxygen bond makes the carbonyl carbon electrophilic.

A

Carbonyl group

19
Q

An amide having the general structure RCONH2.

A

Primary (1°) amide

20
Q

An amide having the general structure RCONHR’.

A

Secondary (2°) amide

21
Q

An amide having the general structure RCONR’2.

A

Tertiary (3°) amide

22
Q

The types of interactions that exist between molecules. Functional groups determine the type and strength of these forces. Intermolecular forces are also called noncovalent interactions or nonbonded interactions.

A

Intermolecular forces

23
Q

Very weak intermolecular interactions caused by momentary changes in electron density in molecules. The changes in electron density cause temporary dipoles, which are attracted to temporary dipoles in adjacent molecules

A

Van der Waals forces

24
Q

A measure of how the electron cloud around an atom responds to changes in its electronic environment.

A

Polarizability

25
Q

An attractive intermolecular interaction between the permanent dipoles of polar molecules. The dipoles of adjacent molecules align so that the partial positive and partial negative charges are in close proximity.

A

Dipole–dipole interaction

26
Q

An attractive intermolecular interaction that occurs when a hydrogen atom bonded to an O, N, or F atom is electrostatically attracted to a lone pair of electrons on an O, N, or F atom in another molecule.

A

Hydrogen bonding

27
Q

The temperature at which molecules in the liquid phase are converted to the gas phase. Molecules with stronger intermolecular forces have higher boiling points. Boiling point is abbreviated as bp.

A

Boiling point

28
Q

The temperature at which molecules in the solid phase are converted to the liquid phase. Molecules with stronger intermolecular forces and higher symmetry have higher melting points. Melting point is abbreviated as mp.

A

Melting point

29
Q

A measure of the extent to which a compound dissolves in a liquid.

A

Solubility

30
Q

The compound that is dissolved in a liquid solvent.

A

Solute

31
Q

The liquid component into which the solute is dissolved.

A

Solvent

32
Q

The principle that compounds dissolve in solvents having similar kinds of intermolecular forces; that is, polar compounds dissolve in polar solvents and nonpolar compounds dissolve in nonpolar solvents.

A

“Like dissolves like”

33
Q

Attracted to water. The polar portion of a molecule that interacts with polar water molecules is hydrophilic.

A

Hydrophilic

34
Q

Not attracted to water. The nonpolar portion of a molecule that is not attracted to polar water molecules is hydrophobic.

A

Hydrophobic

35
Q

Organic compounds needed in small amounts by biological systems for normal cell function.

A

Vitamins

36
Q

Spherical droplets formed by soap molecules having the ionic heads on the surface and the nonpolar tails packed together in the interior. Grease and oil dissolve in the interior nonpolar region.

A

Micelles

37
Q

A hydrolyzable lipid that contains a phosphorus atom.

A

Phospholipid

38
Q

An organic molecule that can form a complex with cations so they may be transported across a cell membrane. Ionophores have a hydrophobic exterior and a hydrophilic central cavity that complexes the cation.

A

Ionophore

39
Q

A cyclic ether containing multiple oxygen atoms. Crown ethers bind specific cations depending on the size of their central cavity.

A

Crown ether

40
Q

An organic compound found in a biological system.

A

Biomolecule