straight chain structure for C6H6 may be CH2=CH-C=C-CH=CH2 (two double and one triple bond) . but if it is so then it should undergo the addition reactions easily.but in actual practice benzene does not undregoes addition reaction easily and not reacts with HCl , Br2 and KMnO4 solutions......
The glass has amorphous structure. It is mean that it made up of very long chain of atoms.
Phenylalanine. When phenylalanine is subjected to a xanthoproteic test, it will produce a yellow solution due to the reaction of the aromatic ring with nitric acid, indicating the presence of phenyl group in the tripeptide.
First Step: Friedel Craft Acylation on benzene to form phenyl methyl ketone or acetophenone. Second Step: Reduction of acetophenone by Clemmenen reduction using zinc amalgam and HCl to give the desired product. Another method is the reaction of benzene with ethyl chloride in presence of AlCl3 and heat in a close container.
FM 1 "The Law of Land Warfare, Uniform Code of Military Justice, and Code of Conduct give structure to its moral standards."
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letse
Benzene has two resonance structures. In the resonance hybrid, each carbon-carbon bond is a hybrid of a single bond and a double bond, resulting in a delocalized pi electron system. This delocalization gives benzene its unique stability and reactivity compared to typical alkenes.
nitration of the benzene ring and gives positive
The glass has amorphous structure. It is mean that it made up of very long chain of atoms.
Nitrobenzene is typically synthesized by nitration of benzene using a mixture of concentrated nitric acid and sulfuric acid as the nitrating agents. The reaction involves the substitution of a hydrogen atom on the benzene ring with a nitro group, resulting in the formation of nitrobenzene.
Benzoic acid will give brisk effervescence on reacting with sodium bicarbonate.
The benzene molecule is unsaturated but the double bonds present inside the benzene ring are delocalized due to bond resonance (pi structure). This makes the double bonds of benzene much less reactive then more discreet double bonds (as in ethylene). This structure makes it behave more like a saturated compound, preferring substitution reactions over addition reactions. It is resistant to addition reactions across the double bond because such a reaction reduces the resonance stabilization energy. However, when reactions do occur, resonance stability is almost always re-established (Birch Reduction reactions are exceptions. See related link).
The structural formula for alcohols is R-OH, where R represents an alkyl group. Alcohols contain a hydroxyl (-OH) group attached to a carbon atom of an alkyl group. The specific structure will vary depending on the alkyl group attached to the hydroxyl group.
Give 3 trivias about in food chain please
Phenylalanine. When phenylalanine is subjected to a xanthoproteic test, it will produce a yellow solution due to the reaction of the aromatic ring with nitric acid, indicating the presence of phenyl group in the tripeptide.
In the 60's, a slang term used by subculture, associated with "give me the straight skinny", a narrow honest truth. Damn straight means no curves or wiggle room, just straight truth. "give me a straight answer"
give it to him straight, he'll give up soon enough. gentil but straight-forward