Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reacrtion involves electroph

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Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This ... (2)` D. `.^(*)C Cl_(3)`

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Description : Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reacrtion involves electroph

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Last Answer : Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. ... ` D. aq. `NaOH + C Cl_(4)`

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Last Answer : Reimer-Tiemann reaction of phenol with cholorform and aqueous alkali takes place through the ... carbanions C. carbon radicals D. carbenes

Description : Phenol is an ortho-para director because the hydroxyl group : (a) donates electrons that increase electron density at ortho and para positions favoring nucleophilic attack. (b) donates ... para positions and attracts electrons away from meta positions favoring electrophilic attack on the ring.

Last Answer : donates electrons that increase electron density at ortho and para positions favoring electrophilic attack.

Description : The product of Reimer-Tiemann reaction is a

Last Answer : The product of Reimer-Tiemann reaction is a A. phenolic aldehyde B. hydroxyamine C. nitroaldehyde D. nitroalcohol

Description : The `-NO_(2)` group in an aromatic ring deactivates the ortho and para positions for an electrophilic attack. When `-NO_(2)` group is present at ortho

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Description : The `-NO_(2)` group in an aromatic ring deactivates the ortho and para positions for an electrophilic attack. When `-NO_(2)` group is present at ortho

Last Answer : The `-NO_(2)` group in an aromatic ring deactivates the ortho and para positions for an electrophilic attack. When ` ... product (H) is : A. B. C. D.

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Last Answer : The `-NO_(2)` group in an aromatic ring deactivates the ortho and para positions for an electrophilic attack. When ` ... product (G) is : A. B. C. D.

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Description : In the reaction of phenol with `CHCl_(3)` and aqueous `NaOH` at `70^(@)`, the electrophile attacking the ring is:

Last Answer : In the reaction of phenol with `CHCl_(3)` and aqueous `NaOH` at `70^(@)`, the electrophile attacking the ring is: ... ` C. `:"CCl"_(2)` D. `COCl_(2)`

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Description : Cyclohexane does not belong to aromatic class even though it has a ring structure. How do you justify this?

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