What happens in Sulphonation?

Sulfonation is a reversible reaction that produces benzenesulfonic acid by adding sulfur trioxide and fuming sulfuric acid. The reaction is reversed by adding hot aqueous acid to benzenesulfonic acid to produce benzene.
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Is sulfonation electron withdrawing?

Due to their electron withdrawing effects, sulfonate protecting groups can be used to prevent electrophilic aromatic substitution. They can also be installed as directing groups to affect the position where a substitution may take place.
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What is sulfonation in organic chemistry?

Sulfonation: A chemical reaction which introduces the sulfonic acid functional group (-SO3H) into a molecule. Sulfonation with sulfur trioxide and sulfuric acid converts benzene into benzene sulfonic acid.
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How is sulphonation done?

The desulphonation which occurs when a sulphonic acid is heated in aqueous acidic solution is an example of the electrophilic replacement (in this case by a proton) of the sulphonic acid group.
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What is electrophile formed during sulphonation?

The formation of the electrophile

Sulfur trioxide is an electrophile because it is a highly polar molecule with a fair amount of positive charge on the sulfur atom.
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Sulfonation of Benzene



What is sulphonation reaction of benzene?

Sulfonation of benzene is a process of heating benzene with fuming sulphuric acid (H2SO4 +SO3) to produce benzenesulfonic acid. The reaction is reversible in nature.
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What is the nucleophile in the sulfonation reaction?

The p electrons of the aromatic C=C act as a nucleophile, attacking the electrophilic S, pushing charge out onto an electronegative O atom.
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What is electrophile in sulphonation of benzene?

So, the active electrophile in sulphonation of benzene is sulphur trioxide.
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What is sulphonation aniline?

Sulphonation. Sulphuric acid reacts vigorously with aniline to form anilinium hydrogen sulphate which on heating produces sulphanilic acid which in turn also has a resonating structure with zwitter ion as shown in the above figure.
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Why is sulphonation reversible?

Sulfonation of benzene is a reversible reaction. Sulfur trioxide readily reacts with water to produce sulfuric acid and heat. Therefore, by adding heat to benzenesulfonic acid in diluted aqueous sulfuric acid the reaction is reversed.
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What is a sulfonation reaction?

Sulfonation is a reversible reaction that produces benzenesulfonic acid by adding sulfur trioxide and fuming sulfuric acid. The reaction is reversed by adding hot aqueous acid to benzenesulfonic acid to produce benzene.
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What is meant by sulphonation?

noun Chemistry. the process of attaching the sulfonic acid group, –SO3H, directly to carbon in an organic compound.
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What is the importance of sulfonation?

Sulfonation plays an essential role in the biotransformation of endogenous compounds such as hormones and neurotransmitters as well as xenobiotics.
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Is sulfation the same as sulfonation?

Sulfonation and sulfation are two important chemical processes used in many industries to add a sulfur-containing group to an organic compound. The main difference between sulfonation and sulfation is that sulfonation involves the formation of a C-S bond whereas sulfation involves the formation of a C-O-S bond.
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What is the electrophile in aromatic sulfonation chegg?

Overview of Aromatic Sulfonation

When an aromatic compound is heated with the sulfuric acid, there will be the formation of an aryl sulfonic acid. It is an electrophilic aromatic substitution reaction in which sulfur trioxide, or the protonated derivative of sulfur trioxide can act as an electrophile.
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What is Sulphonation plant?

Sulphonation Technologies

Technithon specializes in continuous modular and skid based process plants using sulfuric acid, oleums, Air-SO3, Liquid SO2 + SO3 as sulfonating agents. Technithon offer technologies and plants for Anionic surfactants (both water and oil soluble).
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When aniline undergoes sulphonation then which of the following product will form?

Aniline gives p- benzene sulphonic acid (Sulphanilic acid), on sulphonation.
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What happens when chlorobenzene undergoes sulphonation?

So, sulphonation of chlorobenzene gives p-chlorobenzene sulphonic acid and o- chlorobenzene sulphonic acid.
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What happens when aniline undergoes nitration?

In nitration of aniline in strong acid (HNO3, H2SO4) aniline changes to anillium ion . Anillium withdraws electron density. Its effect is felt maximum at ortho followed by meta and then para position. Consequently very little of ortho nitrated product is formed.
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Is the sulphonation of benzene is electrophilic substitution?

The sulfonation of benzene with SO3 is a trimolecular electrophilic substitution. In sulfonic acid or oleum, the trimolecular system is C6H6 + SO3 + H2SO4. H2SO4 is a catalyst.
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Why SO3 is used in sulphonation reaction?

Conventionally sulfonation is done by sulphuric acid or oleum. But with SO3 sulfonation process has the following advantages. It is more direct and considerably faster than the present process. It requires fewer man hours and, therefore, is more economical.
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What reagent is sulfonation?

Sulfonation with oleum and sulfuric acid

Oleum and sulfuric acid are widely used sulfonation and sulfation reagents, although reactions with these reagents require corrosion-resistant materials of construction.
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What is the cofactor in sulfonation?

Sulfonation reactions (also less correctly known as sulfation reactions) consist in a sulfate being transferred from the cofactor 3′-phosphoadenosine 5′-phosphosulfate (PAPS) to the substrate under catalysis by a sulfotransferase.
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What is Sulphonation of phenol?

Sulphonation of phenol is an electrophilic aromatic substitution reaction and is also reversible.
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