10.1 Fundamentals of organic chemistry Flashcards

1
Q

define catenation

A

CATENATION: C ability to form chains and rings - vast number of carbon compounds

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2
Q

Dustinguish saturated vs unsaturated

A
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3
Q

Distinguish aliphatics vs arenes

A
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4
Q

Distinguish electrophile vs nucleophile

A
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5
Q

Dinstinguish addition vs substitution vs addition elimination reactions

A
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6
Q

Types of bond breaking

A
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7
Q

Representation of moving e in reaction mechanisms

A
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8
Q

Alkane general formula

A

CnH2n+2

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9
Q

General formula of alcohols

A

CnH2n+1OH

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10
Q

Features of a homologous series

A
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11
Q

Types of chemical formulas and their characteristics

A
  • full structural
  • condensed structural
  • stereochemical: with 3D projections
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12
Q

Steps of naming an organic compound

A
  1. Identify longest C chain
  2. Identify functional groups (what the compound is)
  3. Identify side chains
  4. Construct the name
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13
Q

define structural isomers

A

STRUCTURAL ISOMERS: molecules that have the same molecular formula but different structural arrangements of the atoms

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14
Q

How are primary, secondary, tertiary compounds identified

A

Primary - 1 C atom bonded to central

Secondary - 2 C atoms bonded to central

Tertiary - 3 C bonded to central

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15
Q

Explain arenes

A

Arenes: compounds derived from benzene, form aromatics branch - contain the phenyl group

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16
Q

Facts on benzene

A
  • no isomer
  • highly unsaturated - ratio of C and H the same - C6H6
  • IUPAC: 1,3,5 - cyclohexatriene
  • very stable due to: equal bonds 120, resonance of delocalised pi e - distributed equaly - minimises repulsion
  • more likely substitution than addition - addition energetically not favoured - disrupts delocalised e cloud
17
Q

Increase in boiling point according to functional group

A