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inn [45]
3 years ago
13

Why is it difficult to undergo nucleophilic substitution in haloarene?​

Chemistry
1 answer:
goldenfox [79]3 years ago
8 0

Answer:

In Haloarenes the C atom to which the X group is attached is SP2 hybridized thus it is become difficult to replace it by the Nucleophile. Since arenes and Vinyl halides are electron rich molecules due to presenceof n bonds, they repel Nucleophile attacking them.

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In the equation given above, there is conservation of MASS, CHARGE AND ENERGY.
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The solubility of three compounds in water is shown in the table above. What best explains the observations shown in the table?
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3 years ago
Over-the-counter hydrogen peroxide solutions are 3% (w/v). What is this concentration in moles per liter?
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3 years ago
Draw the structure for 1-nitrobutane, making sure to add all non-zero formal charges.
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The molecular structure of 1-nitrobutane is C_{4} H_{9} NO_{2}. The structure of 1-nitrobutane is shown below.

An atom's formal charge would be determined by the covalent model of chemical bonding, which assumes that almost all chemical bonds include equal sharing of electrons among all atoms, regardless their relative electronegativity.

The structure for 1-nitrobutane, making sure to add all non-zero formal charges

There are four kind of molecule present in 1-nitrobutane and they are carbon, hydrogen , nitrogen and oxygen. Nitrogen is bonded with two oxygen atom out of them one oxygen atom is attached with single bond and second oxygen atom is bonded with double bond. Nitrogen has positive charge whereas oxygen has negative charge.

It is a kind of alkane in with nitro group is attached with alkane group.

To know more about 1-nitrobutane

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