Give the products formed on heating of 1,1,2-cyclohexane tricarboxylic acid.

First Geminal acid on heating undergo decarboxylation to formed 1,2-Cyclohexane Dicarboxylic acid, which is on further heating gives corresponding anhydride.

Related Questions:

Penta-1,3-diene is more stable than penta-1,4 -diene. Why?

Phenoxide ion is more stable than an alkaoxide. why?

Why does aqueous sodium bicarbonate solution dissolve carboxylic acids but not phenol though they are also acidic ?

Why enol form of Beta Dicarbonyl compound more stable than those of monocarbonyl compounds?

Why enol form of phenol is more stable than its keto isomers?

Reactivity order of Pyrrole, Furan and Thiophene towards Electrophilic substitution :

Phenyl group is known to extract negative inductive effect, but each phenyl ring in biphenyl is more reactive than benzene towards Electrophilic substation. Why?

Chloroform is more acidic than fluoroform why?

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Trifluoroethyl carbocation is less stable than trifluromethyl carbocation why ?

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How can explain that Chloral hydrate is stable Compound although it has two -OH groups attached to same carbon?

Chloral hydrate (CH3-CHO.2H2O) has unusual stability due to -I effect of three Chlorine atoms, which leads to the formation of two Hydrogen bond. The energy released in the formation of three bonds provides extra stability.