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D-erythrose and D-threose both yield the same osazone. Likewise, L-erythrose and L-threose yield the same osazone.

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Q: What are two aldotetroses that yield the same osazone on reaction with phenyl hydrazine?
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What Reagents are used in osazone test?

Reagents of Osazone test are 1. Phenylhydrazine mixture consisting of phenyl-hydrazine and anhydrous sodium citrate 2. Orignal solution containing a carbohydrate


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C6h8n2


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When acetone react with phenylhidrazine equation is phenylhidrazone of acetone, condensation product in which process water molecule eliminate.


What is the mechanism involved in the preparation of glucosazone from glucose?

Desolve 2g of sodiume acetate in 20ml water and place in a round bottom flask. Add 2g phenyl hdrazine hydrochloride in it. Dissolve 1g glucose in 5ml water and addit to the above flask. Heat the flask on water bath for 1 hour. separate the yellow crystals by filtration and wash with acetic acid. GLUCOSE + 3PHENHYL HYDRAZINE HYDROCHLORIDE------->PHENYLE GLUCOSAZONE


What is the mechanism for the reaction of triphenylmethanol with HBr?

Has to be a simple SN1 reaction. tertiary carbocation, very very stable due to three phenyl groups and very bulky.


What is the use of phenyl?

what is the use of phenyl ?


Why is phenylhydrazine a better neuclophile than aniline?

Yes, in phenyl hydrazine the electron pair on terminal nitrogen is always available for attack while in analine the electron pair of nitrogen is less available due to involvement in resonance process with benzene ring.


How do you synthesize 1-phenyl-1-propanol using a grignard reaction?

Reaction of 1-propane-magnesia-bromide with benzaldehyde and destruction of the product with water yields to 1-phenyl-1-propanol.1) 1) Organikum, 21. Aufl., Wiley-VCH Verlag GmbH Weinheim 2001, S. 562


What are the uses of phenyl?

The phenyl is used in the hair care formulations and cosmetics.


Is there radiation in glow sticks?

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What principle of xanthoprotein?

a xanthoprotein is a nitroprotein. The xanthoprotein test is characterisitic reaction of proteins that contain phenyl aromatic function. Nitric acid react with this phenyl group to yellow colored aromatic compound. The yellow stains on the skin from nitric acid exposure is the result of xanthoprotein.


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