Chemistry Semester 3 - Organic Chemistry
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Transcript of Chemistry Semester 3 - Organic Chemistry
![Page 1: Chemistry Semester 3 - Organic Chemistry](https://reader035.fdocuments.net/reader035/viewer/2022082208/58ab597d1a28abbc2a8b4b17/html5/thumbnails/1.jpg)
SEMESTER 3
CHEMISTRY
SEMESTER 3
CHEMISTRY
ORGANIC CHEMISTRY
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Alkane
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Alkene
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Haloalkane
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Hydroxyl compound
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Carbonyl compound
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Carboxyl compound
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Amino compound
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a) Alkane with halogen (X2)
General Equation : RCH2CH3 + X2 (g) → RCHXCH3 + HX
Reagent /Condition : chlorine or bromine gas ;
under ultraviolet light (UV)
Type of reaction : Free radical substitution reaction
Note :Note :
1. The rate of reaction is slow, therefore cannot be use as a test
to distinguish alkane from other compounds.
2. As long as it’s a saturated carbon, it can be halogenated via
free radical reaction. For example :
CH3NH2 + Br2 → BrCH2NH2 + HBr
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b) i.Alkene with halogen (X2)
General equation : RCH=CH2 + X2 (g or l) → RCHXCH2X
Reagent /Condition : chlorine or bromine gas ;
under organic solvent CH2Cl2 or CCl4Type of reaction : electrophilic additional reaction
Note : 1. The rate of reaction is high, and therefore suitable to
be use to distinguish alkene from other functioning group.be use to distinguish alkene from other functioning group.
2. Reaction is slightly different when halogen its reacted as
aqueous solution. For example, when react with bromine water,
the following reaction take place :
RCH=CH2 + Br2 (aq) →
RCH(OH)CH2Br (major) + RCHBrCH2Br (minor)
*Note from the reaction, -OH is added to C with more substituent / Br is added
to C with more H
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b) ii. Alkene with hydrogen halide (HX)
General equation :RCH=CH2 + HX (g) →
RCHXCH3 (major) + RCH2CH2X (minor)
Reagent /Condition : hydrogen chloride, HCl, hydrogen bromide,
HBr / room temperature
Type of reaction : electrophilic additional reactionType of reaction : electrophilic additional reaction
Note : 1. The reaction follows Markovnikoff rules - In addition of
hydrogen halide to unsaturated hydrocarbon, C=C, hydrogen is
preferable to be added to carbon with greater hydrogen in it.
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c) Alcohol with PCl5 or thionyl chloride SOCl2General equation : RCH2OH + PCl5 → RCH2Cl POCl3 + HCl (g)
RCH2OH + SOCl2 → RCH2Cl + SO2 (g) + HCl (g)
Reagent /Condition : PCl5 in room temperature or
SOCl2 under reflux
Type of reaction : nucleophilic substitution reaction.Type of reaction : nucleophilic substitution reaction.
Note :1. Usually the reaction using thionyl chloride is more
preferable since the side products produces are gas, hence the
main organic product is easily isolated.
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d) Carboxylic acid with PCl5 or SOCl2Equation : RCH2COOH + PCl5 → RCH2COCl + POCl3 + HCl (g)
RCH2COOH + SOCl2 → RCH2COCl + SO2 (g) + HCl (g)
Reagent /Condition : PCl5 in room temperature or
SOCl2 under refluxSOCl2 under reflux
Type of reaction : nucleophilic substitution reaction.
Note : 1. Usually the reaction using thionyl chloride is more
preferable since the side products produces are gas, hence the
main organic product is easily isolated.
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e) Benzene (or any derivatives) with halogen
General equation :
Reagent /Condition : chlorine(Cl2) in AlCl3 at room temperature
bromine(Br2) in FeBr3 under refluxbromine(Br2) in FeBr3 under reflux
Type of reaction : electrophilic aromatic substitution reaction.
Note :1. The reaction uses AlCl3 or FeBr3 as catalyst in the
reaction
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f) Phenol with bromine water
General equation :
Reagent /Condition : bromine water, Br2 (aq) under room temp
Type of reaction : electrophilic aromatic substitution reaction.
Note : 1. Observation of the reaction - brown solutionNote : 1. Observation of the reaction - brown solution
decolourised and turned to white precipitate when bromine water
is added to phenol
2. The reaction occur almost immediately since -OH in phenol is
ring activate, which caused all Br to substituted at all ortho and
para position.
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g) Aniline with bromine water
General equation :
Reagent /Condition : bromine water, Br2 (aq) under room temperature
Type of reaction : electrophilic aromatic substitution reaction.Type of reaction : electrophilic aromatic substitution reaction.
Note :1. Observation of the reaction - brown solution decolourised and
turned to white precipitate when bromine water is added to aniline
2. The reaction occur almost immediately since -NH2 in aniline is ring
activate, which caused all Br to substituted at all ortho and para
position.
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Homologous series
Chemical Tests
a)To distinguish alkene from other functioning group
i. Reagent / Condition : bromine in CCl4Observation : Brown colour of bromine decolourised while the other will not
Equation :
ii. Reagent / Condition : hot acidified KMnO4
Alkene
-C=C-
ii. Reagent / Condition : hot acidified KMnO4
Observation : Purple colour of KMnO4/H+ decolourised
while the other will not
Equation :
(Note : This test is also suitable to distinguish alk-1-ene with
other alkene. Both alkene will decolourised purple colour of
KMnO4 but alk-1-ene will further give effervescence that turned line water chalky)
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Alcohol
-C-OH
a) To distinguish 1o, 2o alcohol from tertiary alcohol
i. Reagent : acidified KMnO4 ; under reflux
Observation : purple colour of KMnO4/H+ decolourised
when added to 10 or 2o alcohol, but no observablechanges to 3o alcohol.
Equation
ii. Reagent :acidified K2Cr2O7 under reflux
Observation : green colour of K2Cr2O7/H+ turned orange
when added to 10 or 2o alcohol, but no observablechanges to 3o alcohol.
-C-OHchanges to 3o alcohol.
Equation :
b) ~ Iodoform test.
i. Reagent : I2 /OH- under reflux
Observation : brown colour decolourised and give yellow
crystal precipitate when added to alcohol with -
CH(OH)CH3, while compound without methyl alcoholshows no observable changes
Equation :
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Carbonyl
compoun
a)Distinguish carbonyl compound & other functioning group
i. Reagent / Condition : 2,4-dinitrophenylhydrazine
Observation : Orange precipitate is formed when carbonyl compound is added to 2,4-dinitrophenylhydrazine.
Equation :
compound
C=O
b) To distinguish between aldehyde and ketone
i. Reagent : Fehling solution [solution of complex of Cu2+]
Positive Test : only works for aldehyde (except benzaldehyde)
Observation : blue solution turns to red precipitate of Cu2O
Equation : red ppt.
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ii. Tollens' reagent [solution of complex Ag(NH3)2]+]
Positive test : only work for aldehyde (except glucose)
Observation : colourless solution turn silver mirror
Equation : silver mirror
c) To distinguish between ethanal and other aldehyde / c) To distinguish between ethanal and other aldehyde /
alkan-2-one with other ketone. Reagent : (I2 + NaOH) Iodine in
sodium hydroxide
Only work for ethanal as it has methyl-carbonyl group
Observation : a yellow crystal of triiodomethane is observed
Equation :
CH3CH=O + 3 I2 + NaOH � CHI3 + HCOO–Na+ + 3 HIHI
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Carboxylic acid
-COOH
a) To distinguish between carboxylic acid and otherfunctioning group
Reagent : sodium carbonate, Na2CO3 or sodiumbicarbonate, NaHCO3
Observation : effervescence occur, colourless gas evolved turn lime water chalky
Equation : 2 R-COOH + Na2CO3 �
2 R-COONa + CO2 (g) + H2O
R-COOH + NaHCO � R-COONa + CO (g) + H OR-COOH + NaHCO3 � R-COONa + CO2 (g) + H2O
Amine
R-NH2
a) To distinguish between primary amine and other class ofamine / functioning group
Reagent : NaNO2 + HCl / 0-5oC
Observation : effervescence occur, colourless gas evolved.
Equation : R-NH2 + NaNO2 + HCl �R-OH + N2 + H2O + NaCl
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a) To distinguish between benzene and cycloalkane
Reagent / Condition : conc. HNO3 catalysed by conc H2SO4 under reflux
Observation : Yellow oily liquid is observed when mixed with benzene
Equation :
b) To distinguish between phenol and alkyl alcohol
+ HNO3conc. H2SO4
NO2
+ H2O
b) To distinguish between phenol and alkyl alcohol
Reagent / Condition : bromine water
Observation : brown colour decolourised and white precipitate is
formed almost immediately after the reaction
Equation :
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c) To distinguish between phenylamine and alkyl amine
Reagent / Condition : bromine water
Observation : brown colour decolourised and white precipitate is
formed almost immediately after the reaction
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a) CH3CH2CH2OH to CH3CH2CH2CH2NH2
b) CH3CH2CH2Br to CH3CH2CH(OH)COOH
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c) CH3CH2COOH to CH3CH2CH2COOH
d) CH3CH2OH to CH3CH(OH)CH3
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e) CH3CH2OH to CH3CH2CH2CH2CONHCH2CH3
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Sn, HClCH3
NO2
Cl2, UV
CH3
OH
CH2Cl
OH
ethanolic
KCN
CH2CN
OH
1. LiAlH4
2. H3O+
CH2CH2NH2
OH
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