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Tuesday, January 28, 2020
Monday, January 27, 2020
What is Chloretone ?
The Chemical (IUPAC) name of Chloretone is 1,1,1-trichloropropane-2-ol which is formed by reaction of chloroform and acetone in the presence of strong alkali like KOH.
Chloretone is act as Hypnotic (Sleep inducing agent ).
Related Questions:
What is Phosgene gas ?
Phosgene is a chlorine containing highly poisonous gas, which formed by oxidation of chloroform in the presence of oxygen and sunlight.
To prevent the formation of Phosgene from chloroform following measures are taken
(1) chloroform kept in brown the bottles.
(2) these bottles are filled with capacity to exclude any air.
(3) 0.6. To 1.0% ethyl added to removed Phosgene formed.
Related Questions:
What is Chloretone ?
What is chloropicrin or tear gas and give it's structure and uses ?
How can explain that Chloral hydrate is stable Compound although it has two -OH groups attached to same carbon?
What is Urotropine give the structure and uses of Urotropine?
What Is Mustard Gas?
What is the structure and use of Westron and Westrosol?
DDT- Dichlorodiphenyltrichloroethane:
Amoxicillin:Antibiotics:
Fluoxetine: Antidepressant:
AZT: Azidodeoxythymidine: Drug that treats human immunodeficiency virus (HIV):
Aspirin: Acetylsalicylic acid:
Related Questions:
What is Chloretone ?
What is chloropicrin or tear gas and give it's structure and uses ?
How can explain that Chloral hydrate is stable Compound although it has two -OH groups attached to same carbon?
What is Urotropine give the structure and uses of Urotropine?
What Is Mustard Gas?
What is the structure and use of Westron and Westrosol?
DDT- Dichlorodiphenyltrichloroethane:
Amoxicillin:Antibiotics:
Fluoxetine: Antidepressant:
AZT: Azidodeoxythymidine: Drug that treats human immunodeficiency virus (HIV):
Aspirin: Acetylsalicylic acid:
What is chloropicrin or tear gas and give it's structure and uses ?
Chloropicrin obtained by reaction of chloroform and nitric acid and it causes tears in eyes and therefore it is used in warfare's as tear gas .
Related Questions:
Although both in benzylic carbanion and cyclopentadienyl anion 6 electrons are spread, but benzylic carbanion is more stable. Why?
The answer of this question lies in the fact that in benzylic carbanions 6 electrons are delocalized over six carbon atoms while in cyclopentadienyl anion 6 electrons are delocalized over 5 carbon atoms , so the dispersal is more in former. We know that greater the dispersal, more is the stability, hence Benzylic carbanion is more stable than cyclopentadienyl anion.
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?
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?
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?
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?
Topic:
GENERAL ORGANIC CHEMISTRY
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