It is commonlt known as resist salt which is a mild oxidising agent and used in reactive printing
The derivative of m-dinitrobenzene is 3,5-dinitrobenzene. It has nitro groups at the meta positions on the benzene ring.
nitro group is very electronegative,so it withdraws electron from the benzene ring so as to destabalize the carbocations in the ortho- and para- position. Nitro group is also fairly bulky so steric hinderance limits the formation of ortho product.ok?
ortho-para in benzene is meaningless these positions are for monosubstituted benzene. Meta is positions 3 and 5. Ortho is position 2 and 6 with relation to already attached group, para is 4 (opposite) to attached group.
The end product of nitrobenzene being nitrated at 125 degrees Celsius with mixed acids would be a mixture of meta-nitrobenzene (major product) and ortho-nitrobenzene (minor product). The reaction conditions favor the formation of the meta isomer due to the lower activation energy for the meta position.
The meta position on a benzene ring is significant in organic chemistry because it determines the location of substitution reactions on the ring. Substituents at the meta position affect the reactivity and properties of the compound, influencing its overall structure and function.
The derivative of m-dinitrobenzene is 3,5-dinitrobenzene. It has nitro groups at the meta positions on the benzene ring.
nitro group is very electronegative,so it withdraws electron from the benzene ring so as to destabalize the carbocations in the ortho- and para- position. Nitro group is also fairly bulky so steric hinderance limits the formation of ortho product.ok?
1,3-dimethylbenzene (meta-xylene) forms only one trisubstituted benzene due to its symmetrical structure, where the two methyl groups are in the meta positions with respect to each other on the benzene ring. This symmetry allows for only one possible trisubstituted product to form.
ortho-para in benzene is meaningless these positions are for monosubstituted benzene. Meta is positions 3 and 5. Ortho is position 2 and 6 with relation to already attached group, para is 4 (opposite) to attached group.
The end product of nitrobenzene being nitrated at 125 degrees Celsius with mixed acids would be a mixture of meta-nitrobenzene (major product) and ortho-nitrobenzene (minor product). The reaction conditions favor the formation of the meta isomer due to the lower activation energy for the meta position.
The meta position on a benzene ring is significant in organic chemistry because it determines the location of substitution reactions on the ring. Substituents at the meta position affect the reactivity and properties of the compound, influencing its overall structure and function.
The most reactive site of 2-nitro toluene is its 4th position which is para to methyl group and meta to nitro group.
The prefixes are ortho- (o-), meta- (m-), and para- (p-). These prefixes indicate whether the substituents are located in positions 1 and 2 (ortho-), 1 and 3 (meta-), or 1 and 4 (para-) on the benzene ring.
Sodium hydrogen sulphite: Sodium bisulfite, not sodium "meta" bisulfite
I can't draw images, but I can describe it. The resonance structure of benzene involves a delocalized ring of six carbons with alternating single and double bonds. The structure shows two resonance forms with the double bonds shifting around the ring to maintain stability and equal bond lengths.
Sodium is a meta element. Atomic mass of it is 23.
Sodium is a meta element. Atomic mass of it is 23.