Table of Contents
- 1 What evidence is there for the structure of benzene?
- 2 Which reaction gives the evidence behind the cyclic structure of benzene?
- 3 Why was the structure shown rejected as the structure of benzene c6h6?
- 4 Why is the structure of benzene?
- 5 How did Kekule proposed the structure of benzene?
- 6 How do you establish the aromatic Behaviour of benzene?
- 7 Which of the following is not explained by Kekule structure of benzene?
- 8 Why straight chain of benzene is not possible?
What evidence is there for the structure of benzene?
The most commonly encountered aromatic compound is benzene. The usual structural representation for benzene is a six carbon ring (represented by a hexagon) which includes three double bonds. Each of the carbons represented by a corner is also bonded to one other atom. In benzene itself, these atoms are hydrogens.
Which reaction gives the evidence behind the cyclic structure of benzene?
The most striking evidence to unusual stability of benzene ring is found in the chemical reactions of benzene & the heat released in a hydrogenation reaction of one mole of an unsaturated compound. ✓ Benzene undergoes substitution rather than addition.
What is benzene and its derivatives?
Benzene is an aromatic compound having molecular formulae CH, It contains six carbon atoms, 6-hydrogen atoms and three conjugated double bonds. Aro- matic compounds having one or more benzene rings in their molecules are called benzenoid. compounds or benzenoids.
Why was the structure shown rejected as the structure of benzene c6h6?
In benzene, all of the carbon-carbon bond lengths are equal. Therefore, the Kekule structure shown below is an incorrect representation of benzene. It is incorrect because it suggests that there are two different types of carbon-carbon bonds in benzene, a carbon-carbon double bond and a carbon-carbon single bond.
Why is the structure of benzene?
The six carbon atoms form a perfectly regular hexagon. All of the carbon-carbon bonds have exactly the same lengths – somewhere between single and double bonds. There are delocalized electrons above and below the plane of the ring. The presence of the delocalized electrons makes benzene particularly stable.
Why Kekules structure of benzene is the correct structure?
This structure is known as Kekule structure and it satisfies the observations that: (i) Benzene contains three double bonds. (ii) All the carbon and hydrogen atoms in benzene are equivalent. Hence, only one mono substituted derivative of benzene is possible.
How did Kekule proposed the structure of benzene?
Kekulé was the first to suggest a sensible structure for benzene. The carbons are arranged in a hexagon, and he suggested alternating double and single bonds between them. Each carbon atom has a hydrogen attached to it. This diagram is often simplified by leaving out all the carbon and hydrogen atoms!
How do you establish the aromatic Behaviour of benzene?
Aromaticity of benzene According to Huckel rule, for a ring to be aromatic it should have the following property: Planarity. Complete delocalization of the π electrons in the ring. Presence of (4n + 2) π electrons in the ring where n is an integer (n = 0, 1, 2, . . .)
How are the derivatives of benzene named?
The general format for this kind of naming is: (positions of substituents (if >1)- + # (di, tri.) + substituent)n + benzene. For example, chlorine (Cl) attached to a phenyl group would be named chlorobenzene (chloro + benzene).
Which of the following is not explained by Kekule structure of benzene?
The structure proposed by Kekule was unable to explain the following facts. According to Kekule benzene contains three double bonds, the chemical properties of benzene should resemble those of alkene. But actually it is not so. Benzene is highly stable and forms substitution compounds easily.
Why straight chain of benzene is not possible?
2. Straight chain structure not possible: Benzene could be constructed as a straight chain or ring compound but it not feasible since it does not show the properties of alkenes or alkynes. for example, it did not decolourise bromine in carbon tetrachloride or acidified KMnO4.