3.3.1 Introduction to Organic Chemistry Flashcards

1
Q

saturated

A

contain single carbon-carbon bonds only

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2
Q

unsaturated

A

contains a C=C double bond

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3
Q

molecular formula

A

the formula which shows the actual number of each type of atom

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4
Q

empirical formula

A

shows the simplest whole number ratio of atoms of each element in the compound

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5
Q

general formula

A

algebraic formula for a homologous series

e.g CnH₂n

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6
Q

structural formula

A

shows minimal detail that shows the arrangement of atoms in a molecule

e.g CH₃

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7
Q

displayed formula

A

show all the covalent bonds and atoms present in a molecule

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8
Q

skeletal formula

A

shows the simplified organic formula, shown by removing hydrogen atoms from alkyl chains, leaving just a carbon skeleton and associated functional groups

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9
Q

homologous series

A

families of organic compounds with the same functional group and same general formula

-they show a gradual change in physical properties
-each member differs by CH₂ from the last
-same chemical properties

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10
Q

ALKANE: Functional Group?

A

C—C

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11
Q

ALKANE: Prefix/Suffix?

A

-ane

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12
Q

ALKENE: Functional Group?

A

C==C

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13
Q

ALKENE: Prefix/Suffix?

A

-ene

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14
Q

ALCOHOLS: Functional Group?

A

C—OH

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15
Q

ALCOHOLS: Prefix/Suffix?

A

-ol

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16
Q

HALOGENOALKANES: Functional Group?

A

C—Halogen

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17
Q

HYDROGENOALKANES: Prefix/Suffix?

A

chloro-
bromo-
iodo-

18
Q

ALDEHYDES: Functional Group?

A

O
||
—C—H

19
Q

ALDEHYDES: Prefix/Suffix

A

-al
formyl-

20
Q

KETONES: Functional Group?

A

O
||
—C—

21
Q

KETONES: Prefix/Suffix?

22
Q

CARBOXYLIC ACID: Functional Group?

A

O
||
—C—OH

23
Q

CARBOXYLIC ACID: Prefix/Suffix?

24
Q

ESTERS: Functional Group?

A

O
||
—C—O

25
ESTERS: **Prefix/Suffix**
-yl —oate
26
order of priority, highest first?
1. Carboxylic Acids 2. Nitrile 3. Aldehyde 4. Ketone 5. Alcohol 6. Amine 7. Alkene 8. Halogenoalkane **Anagram**: cry not alien, kill aliens against all happiness
27
2 types of bond breaking/fission
-heterolytic -homolytic
28
**Heterolytic Fission**
-one atom gets both electrons -the atom that gains the electrons becomes **negatively** charged, -the atom that loses an electron becomes **positively** charged e.g H–Br → H⁺ + Br⁻ (*double-headed* arrow going from middle of bond to adjacent element)
29
**Homolytic Fission**
-each atom gets one electron from the covalent bond -this produces **2 free radicals**, (atoms with unpaired electrons) -these free radicals are unstable and therefore highly reactive e.g H–Br → •H+ •Br
30
free radical
reactive species which possess an unpaired electron
31
what will an arrow always start from?
-lone pair -centre of a bond
32
formation of a covalent bond? (arrow start and end)
-starts from lone pair -starts from another covalent bond
33
breaking of a covalent bond? (arrow start and end)
-start from a lone pair -start from centre of bond
34
what are the 2 types of isomers?
-structural -stereoisomers
35
structural isomers
**same** molecular formula **different** structures
36
stereoisomers
**same** molecular formula **same** structure arranged **differently** in space
37
3 examples of *Structural Isomers*
-chain isomerism -position isomerism -functional group isomerism
38
2 examples of *Stereoisomers*
-optical -E-Z
39
What are the functional group isomerism pairs?
-Aldehydes & Ketones -Carboxylic Acids & Esters -Alkenes & Cycloalkanes
40