KIMIA DASAR I APAKAH KIMIA ORGANIK Ilmu yang

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KIMIA DASAR I

KIMIA DASAR I

APAKAH KIMIA ORGANIK ? Ilmu yang mempelajari senyawa -senyawa hidrokarbon dan derivatnya Perbandingan :

APAKAH KIMIA ORGANIK ? Ilmu yang mempelajari senyawa -senyawa hidrokarbon dan derivatnya Perbandingan : 7 million senyawa organik 1. 5 million senyawa anorganik

SENYAWA ORGANIK n Materi tanaman / hewan n Makanan n Bahan farmasi/ kosmetik n

SENYAWA ORGANIK n Materi tanaman / hewan n Makanan n Bahan farmasi/ kosmetik n Plastik n Komponen minyak bumi n Pakaian

Some organic chemicals Medicines DNA • Active Pharmaceutical Ingredients • Excipients Fuels Materials Essential

Some organic chemicals Medicines DNA • Active Pharmaceutical Ingredients • Excipients Fuels Materials Essential oils Pigments

HSenyawa I D R Oyang K Aterdiri RBO N dari karbon dan hidrogen Berdasarkan

HSenyawa I D R Oyang K Aterdiri RBO N dari karbon dan hidrogen Berdasarkan ikatannya Hidrokarbon jenuh Hidrokarbon tak jenuh alkana, alkena, alkuna, benzena

Carbon (C) Unsur kehidupan di atas bumi adalah C MENGAPA ? ? ? memiliki

Carbon (C) Unsur kehidupan di atas bumi adalah C MENGAPA ? ? ? memiliki 4 buah elektron bonding yang dapat membentuk ikatan kovalen yang kuat, dapat berupa ikatan tunggal dan rangkap (2 atau 3)

Molekul organik paling sederhana: Susunan OKTET yang stabil metana Covalent Bonding – Atoms Share

Molekul organik paling sederhana: Susunan OKTET yang stabil metana Covalent Bonding – Atoms Share Electrons

ALKANA

ALKANA

Bentuk dasar Hibridisasi Bentuk tereksitasi 4 sp 3

Bentuk dasar Hibridisasi Bentuk tereksitasi 4 sp 3

Struktur tetrahedral pada metana Carbon yang menunjukkan hibridisasi sp 3 4 buah ikatan C-H

Struktur tetrahedral pada metana Carbon yang menunjukkan hibridisasi sp 3 4 buah ikatan C-H yang ekivalen (ikatan s) Semua ikatan tunggal dinamakan ikatan s

Alkana Cn. H 2 n+2 consist of only carbon and hydrogen bonded by single

Alkana Cn. H 2 n+2 consist of only carbon and hydrogen bonded by single covalent bonds single Skeletal structure of only carbon atoms

Contoh : 2 -metilbutana 3 -etil-5 -metilheksana 3+5=8 4 -etil-2 -metilheksana 4+2=6

Contoh : 2 -metilbutana 3 -etil-5 -metilheksana 3+5=8 4 -etil-2 -metilheksana 4+2=6

SIFAT FISIK n n n n Senyawa non polar, densitas <1, dengan air membentuk

SIFAT FISIK n n n n Senyawa non polar, densitas <1, dengan air membentuk dua lapisan Larut dalam pelarut organik non polar Alkana C 4, berbentuk gas, Alkana Mr >, berbentuk cair, Alkana Mr >>>, berbentuk padat Semakin besar jumlah atom C, Mr molekul semakin >, gaya dispersi tiap molekul >, titik didih semakin tinggi Alkana bercabang td < alkana rantai lurus padanannya Ada pengaruh gaya van der Waals antar molekul Ikatan tunggal mampu berotasi bebas

Melting (blue) and boiling (pink) points of the first 14 n-alkanes in °C.

Melting (blue) and boiling (pink) points of the first 14 n-alkanes in °C.

Isomers – the have the same molecular formula, but a different structures Structural Isomers

Isomers – the have the same molecular formula, but a different structures Structural Isomers – same molecular formula, but atoms are bonded in different orders. C 4 H 10 – has two isomers, n-butane and isobutane (2 -methylpropane) Has the same molecular formula as n-pentane, C 5 H 12 (2 -methylbutane) Has different Physical Properties : m. p, b. p. density (2, 2 -dimethylpropane)

CYCLOALKANES Cn. H 2 n

CYCLOALKANES Cn. H 2 n

Cyclopropane Bond angles 60° Cyclobutane Bond angles 88° Cyclopentane Bond angles 108° Cyclohexane Bond

Cyclopropane Bond angles 60° Cyclobutane Bond angles 88° Cyclopentane Bond angles 108° Cyclohexane Bond angles 109. 5°

metilsikloheksana tert-butilsiklopentana 1, 2 -dimetilsikloheksana

metilsikloheksana tert-butilsiklopentana 1, 2 -dimetilsikloheksana

How to draw Cyclohexane ? put in axial H’s put in equitorial H’s

How to draw Cyclohexane ? put in axial H’s put in equitorial H’s

REACTIONS OF ALKANES Combustion Dehydrogenation Halogenation – radical substitution reactions

REACTIONS OF ALKANES Combustion Dehydrogenation Halogenation – radical substitution reactions

Halogenation Substitution Reaction – a reaction in which part of a small reacting molecule

Halogenation Substitution Reaction – a reaction in which part of a small reacting molecule replaces an atom or a group of atoms on the organic molecule

Alkyl Halides or Haloalkanes 6/5/2021 22

Alkyl Halides or Haloalkanes 6/5/2021 22

Naming them Tend to be Heavier than water More Toxic than Alkanes Tetrachloromethane or

Naming them Tend to be Heavier than water More Toxic than Alkanes Tetrachloromethane or carbon tetrachloride 2 -Chloro-3 -methylbutane 1 -Ethyl-2 -fluorocyclohexane Trichlorofluoromethane (Freon-11) 1 -Bromobutane 3 -Bromo-1 -chlorobutane 2 -Chloropropane or Isopropyl chloride Dichlorodifluoromethane 1, 1, 1, 2 -Tetrafluoroethane (Freon-12) Chlorofluorocarbons (CFCs) Refrigerant Gases, Ozone Depletion, More H’s more degradable

dd+ X is readily displaced by nucleophiles Nu Electronegativity is defined as the ability

dd+ X is readily displaced by nucleophiles Nu Electronegativity is defined as the ability of atoms to attract shared electrons in a covalennt bond ------ leads to nucleophilic substitution in alkyl halides Symmetrical molecules have no dipole moment or have equal distribution of electrons within covalent bonds Therefore, they are unreactive!

STEREOCHEMISTRY 6/5/2021 25

STEREOCHEMISTRY 6/5/2021 25

Isomers are different compounds that have the same molecular formula Structural isomers are isomers

Isomers are different compounds that have the same molecular formula Structural isomers are isomers that differ because their atoms are connected in a different order CH 3 OCH 3 ---- dimethyl ether and CH 3 CH 2 OH ---- ethanol Stereoisomers differ only in the arrangement of their atoms in space Geometric Isomers

Enantiomers are stereoisomers whose molecules are nonsuperimposable mirror images of one another Involves a

Enantiomers are stereoisomers whose molecules are nonsuperimposable mirror images of one another Involves a tetrahedral sp 3 atom

One structure can be superimposed on another If any of the groups attached to

One structure can be superimposed on another If any of the groups attached to the tetrahedral atom are the same, the centre is achiral. The ultimate way to test for molecular chirality is to construct models of the molecule and its mirror image and then determine whether they are superimposable Screwdriver is achiral Socks are achiral Golf club is chiral Gloves are chiral

Properties of Enantiomers have identical melting points and boiling points Enantiomers have identical solubilities

Properties of Enantiomers have identical melting points and boiling points Enantiomers have identical solubilities in solvents Enantiomers have identical spectra and refractive index Enantiomers interact, and react with achiral molecules in the same manner Enantiomers interact and react with other chiral molecules at different rates Enantiomers rotate plane-polarised light by equal amounts but in opposite directions Chiral molecules are optically active Polarimeter is a devise used to measure the effect of planepolarised light on an optically active compound

No Correlation between the direction of rotation of plane polarised light and the absolute

No Correlation between the direction of rotation of plane polarised light and the absolute configuration of a molecule Clockwise Rotation (+) – dextrorotatory Anti-Clockwise Rotation (-) – levorotatory An equimolar mixture of two enantiomers is called a Racemic Mixture It is Optically Inactive 6/5/2021 30

6/5/2021 31

6/5/2021 31