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[HgI4]-(aq) reacts with the lone pairs of nitrogen that are present, then the typical off-white precipitate falls out. A uncharged Mercury salt is thus obtained. In some alkaloids there isn't a reaction with Mayer's reagent because it lacks lone pairs (example berberine) and it reacts also with alkaline peptides. This mechanism is actually similar then Dragendorff's reagent.

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What is the reaction mechanism between an acid chloride and a Grignard reagent?

The reaction mechanism between an acid chloride and a Grignard reagent involves the nucleophilic addition of the Grignard reagent to the carbonyl carbon of the acid chloride, followed by the elimination of the chloride ion to form a ketone. This reaction is known as the Grignard reaction.


What is the mechanism of the reaction between Tollens reagent and aldehydes to form a silver mirror?

The reaction between Tollens reagent and aldehydes to form a silver mirror is a redox reaction. The aldehyde reduces the silver ions in the Tollens reagent to form elemental silver, which then deposits on the surface of the reaction vessel, creating a mirror-like appearance.


What is the mechanism of the reaction between phenyl Grignard reagent and a carbonyl compound?

The reaction between a phenyl Grignard reagent and a carbonyl compound involves the nucleophilic addition of the phenyl group to the carbonyl carbon atom. This forms an alkoxide intermediate, which then undergoes protonation to yield the final alcohol product.


What is the reaction mechanism for the synthesis of 2-bromobutane using NAI as the reagent?

In the synthesis of 2-bromobutane using NAI as the reagent, the reaction mechanism involves the substitution of a bromine atom for a hydroxyl group on butanol. This reaction follows an SN2 mechanism, where the nucleophile (bromine) attacks the carbon attached to the hydroxyl group, leading to the formation of 2-bromobutane.


What is the mechanism of the reaction between lithium and a Grignard reagent, specifically focusing on the role of lithium in the formation of the Grignard reagent?

When lithium reacts with a Grignard reagent, it acts as a catalyst by initiating the formation of the Grignard reagent. The reaction involves the transfer of an alkyl or aryl group from the Grignard reagent to the lithium, resulting in the formation of a new carbon-carbon bond. This process is crucial for the synthesis of various organic compounds in organic chemistry.

Related Questions

What is the mechanism of reaction between Wagner's reagent and alkaloids?

what is the reaction mechanism between wagner's reagent and alkaloids


What is the reaction mechanism between an acid chloride and a Grignard reagent?

The reaction mechanism between an acid chloride and a Grignard reagent involves the nucleophilic addition of the Grignard reagent to the carbonyl carbon of the acid chloride, followed by the elimination of the chloride ion to form a ketone. This reaction is known as the Grignard reaction.


What is the mechanism of the reaction between Tollens reagent and aldehydes to form a silver mirror?

The reaction between Tollens reagent and aldehydes to form a silver mirror is a redox reaction. The aldehyde reduces the silver ions in the Tollens reagent to form elemental silver, which then deposits on the surface of the reaction vessel, creating a mirror-like appearance.


What is the mechanism of the reaction between phenyl Grignard reagent and a carbonyl compound?

The reaction between a phenyl Grignard reagent and a carbonyl compound involves the nucleophilic addition of the phenyl group to the carbonyl carbon atom. This forms an alkoxide intermediate, which then undergoes protonation to yield the final alcohol product.


What is the reaction mechanism for the synthesis of 2-bromobutane using NAI as the reagent?

In the synthesis of 2-bromobutane using NAI as the reagent, the reaction mechanism involves the substitution of a bromine atom for a hydroxyl group on butanol. This reaction follows an SN2 mechanism, where the nucleophile (bromine) attacks the carbon attached to the hydroxyl group, leading to the formation of 2-bromobutane.


What is the mechanism of the reaction between lithium and a Grignard reagent, specifically focusing on the role of lithium in the formation of the Grignard reagent?

When lithium reacts with a Grignard reagent, it acts as a catalyst by initiating the formation of the Grignard reagent. The reaction involves the transfer of an alkyl or aryl group from the Grignard reagent to the lithium, resulting in the formation of a new carbon-carbon bond. This process is crucial for the synthesis of various organic compounds in organic chemistry.


What reagent is necessary to complete the reaction?

The reagent needed to complete a reaction depends on the specific reaction being carried out. It could be a catalyst, solvent, substrate, or a specific chemical compound required for the reaction to proceed successfully. Consulting the reaction mechanism or the experimental protocol would help identify the necessary reagents.


What is the mechanism of the conversion of salicylamide to iodosalicylamide?

The conversion of salicylamide to iodosalicylamide involves the substitution of a hydrogen atom with an iodine atom in the presence of an iodine-containing reagent. This reaction is known as an iodination reaction.


What is the mechanism of the reaction between Wagner's reagent and an alkaloids?

Wagner's reagent, which is an aqueous solution of iodine and potassium iodide, reacts with alkaloids containing nitrogen atoms to form a brown complex. This reaction is based on the oxidation of the nitrogen atoms in the alkaloids by iodine, resulting in the formation of the colored complex. The intensity of the brown color can be used to detect the presence of alkaloids in a given sample.


What is the reaction mechanism of the formation of a precipitate when using the sn/hcl reagent in a chemical test?

When using the Sn/HCl reagent in a chemical test, the reaction mechanism for the formation of a precipitate involves the reduction of tin ions by hydrochloric acid, leading to the formation of tin chloride. This tin chloride reacts with the target analyte in the solution, forming a solid precipitate that can be observed visually.


What is limited reagent?

In a chemical reaction the limiting reagent is the compound totally consumed when the reaction is complete.


What is the equation for the reaction between tollens' reagent and butanone?

The reaction between Tollens' reagent (Ag(NH3)2+) and butanone forms a silver mirror on the inner surface of the reaction vessel. The equation for this reaction is: Ag(NH3)2+ (aq) + 2e- -> Ag(s) + 2NH3(aq)