What is Urotropine give the structure and uses of Urotropine?

Urotropine is nitrogen containing bicycling Compound it's chemical name is Hexamethylenetetramine which is formed by reaction of formaldehyde with ammonia. Urotropine is used as urinary antiseptic.

It is also used for preparation of Cyclonite Research and Development Explosive(RDX).

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Although anti conformation is more stable than the gauch conformation but in some cases gauch or skew conformation is more stable than the anti confirmation why?

Gauch or skew conformation is more stable than the anti because of the intramolecular hydrogen bonding which is geometrically possible only in the gauch conformation.

For examples:

Ethane-1,2-diol, 2-Fluoroethan-1-ol, 2-chloroethan-1-ol and 2-Aminoethanol etc.
2-chloroethane-1-ol:

Ethane-1,2-diol:

Realated Questions:

How many cyclic isomers possible of (C6H12) Hexene?

How many cyclic isomers possible of (C5H10) pentene?

Write the major and minor product of hydration of 1-Methylcyclopent-1-ene in acidic medium?

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?

What is fries rearrangment acylation ?

Conversion of phenolic esters of aliphatic and aromatic carboxylic acids into ortho- and para-acylphenols in the presence of FCR catalyst (AlCl3). Is know as Fries rearrangement.

Related questions:
What is difference between Houben–Hoesch acylation reaction and Gatter- mann–Koch formylation reaction? 

More reated 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?

Fluorine is more electronegative than chlorine even then, p-flurobenzoic acid is weaker acid than p-chlorobenzoic acid explain ? 

Trifluoroethyl carbocation is less stable than trifluromethyl carbocation why ?

Why is the Tropylium carbocation less stable than the tricyclopropylmethyl carbocation?