Alkynes
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Transcript of Alkynes
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Alkynes
C ≡ C
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Alkynes are……..• Aliphatic
hydrocarbons with one triple bond between carbons
• unsaturated hydrocarbons and are generally very reactive. Typical reactions involve the addition of hydrogens or halogens.
• traditionally known as acetylenes or the acetylene series
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General Formula
CnH2n-2
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Alkynes PreparationThe carbon-carbon triple bond of the alkynes is formed in the same
way as a double bond of the alkenes, by the elimination of
atoms or groups from two adjacent carbons. CH3 — CH3 -------→ CH2 ═ CH2 -------→ CH ≡ CH
Alkane Alkene Alkyne
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Alkynes Physical Properties• They are insoluble in water. • They are quite soluble in the usual organic
solvents of low polarity (e.g. ligroin, ether, benzene, carbon tetrachloride, etc.).
• They are less dense than water. • Their boiling points show the usual increase
with increasing carbon number. • They are very nearly the same as the boiling
points of alkanes or alkenes with the same carbon skeletons.
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Structure:The carbon atoms in an
ALKYNE bond are “sp”
hybridized.
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Example:
HC ≡ CHEthyne
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Example:
CH3—C ≡ CH1 – Propyne
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Example:
CH3 – C ≡ C – CH3
2 - Butyne
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NomenclatureWhat is IUPAC Nomenclature?
IUPAC nomenclature is a system of naming chemical
compounds and of describing the science of chemistry in general. It is developed and kept up to date under the support of the International Union of
Pure and Applied Chemistry (IUPAC).
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How to name an alkyneStep # 1
Determine the “ longest continuous chain “of carbons that have the triple bond between two of its carbons. The "longest continuous chain“ does not necessarily have to be straight.
CH2 — C ≡ C — CH2│ │CH3 CH2CH3
3 - heptyne
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How to name an alkyne
Step # 2Number the carbons in the chain so that the triple bond would be between the carbons with the lowest designated number. If it makes no difference to the triple bond then shift attention to the branched groups.
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Example :
CH3 — CH — C ≡ C — C — CH3│ │
│
CH3 CH3
CH3
2,2,5 – trimethyl – 3 – hexyne
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How to name an alkyneStep # 3
Identify the various branching groups attached to this
continuous chain of carbons by name. If two or more alkyl group
are attached to the chain alphabetize, then drop the “ane”
suffix add “yne” to the name.
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Example :
CH3 — CH2 — C — CH2 — C ≡ C — C — CH2 — CH3
│
│
│
│
CH3
CH2 — CH3
CH3 — CH2
CH3
3,7 – diethyl – 3,7 – dimethyl – 4 - nonyne
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1 – cyclobutyne
BrCl
3 – bromo – 6 – chloro – 1,4 – cyclohexadiyne
CH2CH33HC
4 – ethyl – 4 – methyl – 1 – cyclopentyne
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CH2 = CH — C ≡ C — CH2 — CH3
1 – hexen – 3 – yne
CH ≡ C — CH = CH — CH2 — CH3
3 – hexen – 1 – yne
CH2 = CH — CH2 — CH2 — C ≡ CH1 – hexen – 5 – yne
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CH2 = CH — C ≡ C — CH = CH2
1,5 – hexadien – 3 – yne
HC ≡ C — CH = CH — C ≡ CH3 – hexen – 1,5 – diyne
HC ≡ C — CH = CH — C ≡ C — CH = CH2
1,5 – octadien – 3,7 – diyne
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1 – cyclobuten – 3 – yne
BrCl
3 – bromo – 6 – chloro – 1 – cyclohexen – 4 – yne
C ≡ C — C = C — C ≡ C — C = CH2
Br
Cl
Br
Cl5,8 – dibromo – 2,6 – dichloro – 1,5 – octadien – 3,7 – diyne
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Chemical PropertiesUnlike alkanes, alkynes are unstable and
very reactive. This gives rise to the intense heat (>3000 °C) of the acetylene flame used in welding.
The chemical behavior of the alkynes is characterized by their capacity of giving addition reactions, polymerization reactions and metallic derivates forming reactions. A great part of reactions are known as belonging to acetylene.
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Addition Reaction Is a type of chemical reaction in which a compound adds to a multiple bond. In the case of addition reaction take place in ALKYNES, one bond in the triple bond is broken in order to form new bonds.
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Alkyne Addition Reaction Combustion Halogenation Hydrogenation Hydrohalogenation Hydration Polymerization
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Combustion ReactionHydrocarbon + O2 ---------------→ CO2 + H2O
Examples :2 C2H2 + 5 02 -------→ 4 CO2 + 2 H2O
C3H4 + 4O2 -------→ 3CO2 + 2H2O
2C4H6 + 11O2 -------→ 8CO2 + 6H2O
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Halogenation ReactionAlkyne + Halogens -------→ Haloalkene -------→ Haloalkane
Example:
CH ≡ CH + Cl2 ------→ CHCl ═ CHCl + Cl2 ------→CHCl2 — CHCl2
Ehyne 1,2 - dichloroethene 1,1,2,2 - tetrachloroethane
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Example:
+ 2 Br2--------→
Br Br
Br
Br
1,1,2,2 – tetrabromocyclopentane
CH ≡ C — C — CH3 + 2F2 -------→ HC — C — C —CH3
│
│
CH3
CH3
│
│
│
│
F CH3
F CH3
│
│
F
F
1,1,2,2 – tetraflouro – 3,3 – dimethylbutane
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Hydrogenation ReactionAlkyne + Hydrogen --------→ Alkene -------→ Alkane
Example :
CH ≡ CH + 2H2 -------→ CH2 ═ CH2 -------→ CH3 — CH3
Ethyne Ethene Ethane
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Example: :
+ 2H2--------→
Cyclobutyne Cyclobutane
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HydrohalogenationAlkyne + Hydrogen halides ------→ Haloalkene -------→ Haloalkane
Example:
CH3 — C ≡ CH + 2HCl --------→ CH3 — C — CH3
│
│
Cl
Cl2, 2 - dichloropropane
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HydrationAlkyne + H2O -------→ Aldehyde or Ketones
Example:
CH ≡ CH + H2 — O -------→ H — C — C — H
│
│
H
H
║O
Ethanal / (Acetaldehyde)
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Example:
CH3 — C ≡ CH + H2 — O -------→ CH3 — C — CH3
║O
2 – Propanone
(dimethylketone)
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Example:
+ H2 — O -------→ ║
OCyclopentanone
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- Fin -