1---
2geometry: a4paper, margin=2cm
3header-includes:
4- \usepackage{mhchem}
5- \usepackage{chemfig}
6- \usepackage{tabularx}
7---
8
9# Organic Chemistry
10
11Large number of compounds due to:
12
13- 4 valence pairs
14- single / double / triple bonds
15- cyclic (ring) structures
16
17## Properties of hydrocarbons
18
19- *Saturated* - all C-C bonds are single
20- Insoluble in water
21- Almost non-polar (similar electronegativities)
22- Only dispersion forces (valence e-)
23- Dispersion forces increase with length
24- Branched molecules have lower density
25
26## Linear (aliphatic)
27
28Alkanes: \ce{C_{$n$} H_{$2n+2$}}
29Alkenes: \ce{C_{$n$} H_{$2n$}}
30Alkynes: \ce{C_{$n$} H_{$2n-2$}}
31
32## Naming hydrocarbons
33
34- Branches end with _-yl_
35- Indicate number of branches with di-, tri- etc.
36- Longest unbranched carbon chain includes function group
37
38## Functional groups
39
40\setchemfig{atom sep=2em}
41\renewcommand{\arraystretch}{3}
42\begin{tabularx}{0.5\textwidth}{rlX}
43 \hline
44 Alcohols & \ce{-OH} & \chemfig{{\color{blue}R}-OH}\\\hline
45 Esters & \ce{-OCO-} & \chemfig{{\color{blue}R}-C(=[:-30]O)-[:30]O-{\color{blue}R}}\\\hline
46 Aldehydes & \ce{-CHO} & \chemfig{{\color{blue}R}-C(-[:-30]H)=[:30]O}\\\hline
47 Ketones & \ce{-CO-} & \chemfig{C(-[:150]{\color{blue}R})(-[:-150]{\color{blue}R})=O}\\\hline
48 Carboxylic acids & \ce{-COOH} & \chemfig{{\color{blue}R}-C(=[:-30]O)-[:30]O-H}\\\hline
49 Ethers & \ce{-O-} & \chemfig{{\color{blue}R}-[:210]O-[:-30]{\color{blue}R}}\\\hline
50 Amines & \ce{-NH2} & \chemfig{{\color{blue}R}-N(-[:-30]H)(-[:30]H)}\\\hline
51 Amides & \ce{CO-NH} & \chemfig{{\color{blue}R}-[:30]C(=[:90]O)-[:-30]N(-[:30]H)(-[:-30]H)}\\\hline
52\end{tabularx}
53
54
55## Isomers
56
57* **Structural isomers** - same molecular formula, different arrangement
58* **Stereoisomers** - same structural configuration, different orientation
59 * **Opotical isomers** - chiral centre, 4 groups bonded to C, non-superimposable mirror image
60 * **Geometric isomers** - \ce{C=C} double bond, 2 groups bonded to carbon atoms
61 + **Cis** - same horizontal plane
62 + **Trans** - diagonal
63
64\begin{center}\setlength\tabcolsep{1cm}
65\begin{tabularx}{0.5\textwidth}{cc}
66 cis & trans \\
67 \chemfig{[:60]{\text{\color{blue}R$^\prime$}}-C(-[:120]{\text{\color{red}R}})=[0]C(-[:-60]{\text{\color{blue}R$^\prime$}})-[:60]{\text{\color{red}R}}} &
68 \chemfig{[:60]{\text{\color{blue}R$^\prime$}}-C(-[:120]{\text{\color{red}R}})=[0]C(-[:-60]{\text{\color{red}R}})-[:60]{\text{\color{blue}R$^\prime$}}}
69\end{tabularx}\end{center}
70
71## Reactions
72
73**Cracking** - split moluecules with heat/pressure/catalyst
74
75### Alkanes
76
77- Relatively inert
78- Non-polar solvent
79- Non-soluble in \ce{H2O}
80- Combusts in \ce{O2} (forms \ce{CO2 + H2O})
81- Reacts with halogens (**substitution** of \ce{H})
82
83### Alkenes
84
85- More reactive than alkanes
86- **Addition reactions**: \ce{C=C} bond is broken (energy released)
87- **Addition polymerisation**
88
89### Alcohols
90
91- Can be formed from haloalkane substitution reaction
92- **Oxidation** (combustion)
93- Oxidation state $\propto$ no. of atoms connected to \ce{C}
94- **Substitution** of functional group, e.g. \ce{ROH + NH3 -> RNH2 + H2O}
95- Primary alcohols oxidise to aldehydes then carboxylic acids
96- Secondary alcohols oxidise to ketones
97
98### Carboxylic acids
99
100- Weak acids
101- **Hydrolysis**: \ce{RCOOH + H2O <=> RCOO^{-} + H2O^{+}}
102- Rxn with amines - carboxylic acid + amine $\rightarrow$ ammonium salt $\rightarrow$ amide + water
103
104### Esterification
105
106- **Condensation reactions** (esterification): \ce{RCOOH + R^{$\prime$}OH -> RCOOR^{$\prime$} + H2O}
107- This is reversed by **hydrolysis**: ester + water $\rightarrow$ carboxylic acid + alcohol
108- Polyesters