How to prepare an alkane or a cycloalkane from hexanedioic acid??
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An alkane is a simple organic compound that consists of only hydrogen and carbon bonded with only single bonds between carbon atoms. Alkanes are of three types: linear, branched and cycloalkanes.
Cycloalkanes are alkanes in which the carbon atoms join to form a ring.
Hexanedioic acid is a dicarboxylic acid, also called Adipic acid.
Sodium or potassium salt of a dicarboxylic acid during electrolysis gives an alkene. An alkene is generated when an aqueous solution of sodium or potassium salt of a dibasic acid (with adjacent carboyxlic groups) is electrolyzed.
Formula: 2H2O+2e−→2OH−+H2(g)
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Dear student,
● Answer -
Hexanedioic acid on electrolysis by Kolbe reaction gives cyclobutane.
● Explaination -
Hexanedioic acid is shown by formula HOOC-(CH2)4-COOH.
Hexanedioic acid on electrolysis by Kolbe reaction gives cyclobutane.
At anode -
-OOC-(CH2)4-COO- --> C4H8 + 2CO2 + 2e-
At cathode -
2H+ + 2e- --> H2
* The reaction involves decarboxylation of dicarboxylic acid to form cycloalkane.
Hope this helped...
● Answer -
Hexanedioic acid on electrolysis by Kolbe reaction gives cyclobutane.
● Explaination -
Hexanedioic acid is shown by formula HOOC-(CH2)4-COOH.
Hexanedioic acid on electrolysis by Kolbe reaction gives cyclobutane.
At anode -
-OOC-(CH2)4-COO- --> C4H8 + 2CO2 + 2e-
At cathode -
2H+ + 2e- --> H2
* The reaction involves decarboxylation of dicarboxylic acid to form cycloalkane.
Hope this helped...
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