Organic chemistry Flashcards

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1
Q

Organic Compounds

A

Contain CARBON bonded to HYDROGEN
- over 90% of all compounds
EX: carbohydrates, plastics, synthetic fibres, lipids, petroleum, dyes

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2
Q

Properties of Organics Compounds

A
  • covalent bonding
  • low mp and bp
  • variable states of matter (at room temp)
  • most: insoluble in polar solvents
  • non-conductors in solution form
  • react with oxygen to produce CO2, H2O, energy
  • may have isomers
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3
Q

Inorganic Compounds

A

Do not contain Carbon bonded to Hydrogen
- less than 10%
EX: water, salt, polyatomic compounds, cyanides, carbonates

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4
Q

Properties of Inorganic Compounds

A
  • ionic bonding
  • high mp and bp
  • solid form (at room temp)
  • soluble in polar solvents
  • conductors in solution form
  • do not react wth O2
  • no isomers
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5
Q

Carbon

A

Foundation for life:
- bonding capacity of 4 (4 valence electrons) = 4 covalent bonds
- forms bonds with itself and other atoms
- atoms join together to form chains and rings
- variety of bonds (single, double, triple)

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6
Q

Hydrocarbons

A

Organic compounds composed of carbon and hydrogen
- backbone of all organic compounds
- nonpolar, insoluble in water
- Aliphatic and Aromatic

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7
Q

Aliphatic

A

Chains and rings
- alkanes
- alkenes
- alkynes

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8
Q

Aromatic

A

Based on benzene
C6H6

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9
Q

Saturated

A

Containing only single bonds

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10
Q

Unsaturated

A

Containing a double/triple bond

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11
Q

Alkane

A

C(n)H(2n+2)
Naming: suffix “ane”
- saturated
- nonpolar
- unreactive

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12
Q

Alkene

A

C(n)H(2n)
Naming: suffix “ene”
- unsaturated
- nonpolar
- slightly reactive

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13
Q

Alkyne

A

C(n)H(2n-n)
Naming: suffix “yne”
- unsaturated
- nonpolar
- reactive

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14
Q

Cyclic Hydrocarbons

A

C(n)H(2n) - alkanes
Naming: prefix “cyclo” suffix “ane/ene”
- nonpolar
- unreactive

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15
Q

Aromatic (benzene)

A

C6H6
______benzene
- nonpolar
- unreactive
- solvent (lipids)

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16
Q

Alcohol

A

R-OH
Naming: suffix “ol” or prefix “hydroxy”
- polar (H-bond)

17
Q

Aldehyde

A

R-COH
Naming: suffix “al”
- polar (permanent dipole)

18
Q

Ketone

A

R-CO-R
Naming: suffix “one”
- polar (dipole)

19
Q

Carboxylic Acid

A

R-COOH
Naming: suffix “oic acid”
- most polar functonal group
- weak acid (H+ donor)

20
Q

Ester

A

R-COO-R
Naming: alcohol C# suffix “yl”, acid C# suffix “oate”
- polar (dipole)
- formed from alcohol + carboxylic acid)

21
Q

Ether

A

R-O-R
Naming: methylethyl ether or methoxyethane
- polar (dipole)

22
Q

Mercaptan

A

R-SH (thiol)
- polar

23
Q

Amine

A

R-NH2
Naming: prefix “amino”
- polar (dipole, H-bonding)
- weak base (H+ receiver)

24
Q

Amide

A

R-CONH2
Naming: suffix “amide”

25
Q

Anhydride

A

R-CO-O-CO-R

26
Q

Organic Halide

A

R-X (halogen)
Naming: halogen - “ine” + “o” (chlorine = chloro)
- polar (dipole at halogen)

27
Q

Phosphate

A

PO4 (3-)
- negative charge

28
Q

Functional Groups

A

Groups that dictate the overall function of the molecule.
Small units where reactions occur.
Dictate the chemical/physical properties