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The reaction between acetylene and ammoniacal AgNO3 results in the formation of A silver in the class 11 chemical JEE_Main.
With ammoniacal silver nitrate, which of the following compounds will have a reaction?
To produce a silver mirror, aldehydes, such as acetaldehyde and formaldehyde, combine with Tollen’s reagent, which is an ammoniacal solution of silver nitrate.
Which of the following is produced by the reaction of ammonical silver nitrate with acetylene?
The formation of white ppt of disilveracetylide takes place when acetylene gas is introduced into an ammoniacal silver nitrate solution. – White ppt of disilveracetylide is produced when acetylene is heated and then passed over an ammoniacal silver nitrate solution.
What is the result of the reaction between ethyne and ammonical silver nitrate?
What results can be expected from the treatment of acetylene with ammoniacal silver nitrate solution? There is the formation of a white precipitate. When HBr is added to propene, the resulting reaction produces 2-broniopropane; however, when benzoyl peroxide is present, the same reaction produces 1-bromopropane as the product.
What exactly is agNO3 ammonical?
You are inquiring about a solution that contains ammoniacal silver nitrate. Enter Your Name: Put Your Email Address Here: Your Question Is: This alkaline solution, which is sometimes referred to as Tollens’ Reagent, is put through a test to determine whether or not aldehydes are present. In addition, you can use this reagent to put a silver mirror coating to any clean glassware.
Which of the following will not react when exposed to a solution of ammonium silver nitrate:
28 questions found in related categories
What byproducts are produced when acetylene is reacted with silver nitrate?
We are aware that silver acetylide is produced when acetylene is subjected to the Tollens test in conjunction with ammoniacal [AgNO3]…. It is necessary for us to be aware that the Tollens test is utilized in order to detect whether or not hydrocarbons include a triple bond. As a result, we can reach the conclusion that choice A is the appropriate response to the question.
What byproducts are produced as a result of the reaction between ethyne and ammonical cuprous chloride solution?
Both ethene and ethyne have double bonds, while ethyne also contains triple bonds. Among these chemicals, those that react with ammoniacal cuprous chloride include ethyne and acetylene…. -As a result, ethyne is the compound that undergoes a reaction with ammoniacal cuprous chloride that results in the formation of a red precipitate. Thus, the correct answer is choice (C), which is ethyne.
What kind of a reaction does ethyne have with tollens’ reagent?
The reaction between the acidic ethyne and the basic Tollen’s Reagent (ammonium silver nitrate) results in the production of ppt of silver acetylide. This reaction can only take place in the presence of terminal alkynes.
Does Propyne give tollens test?
$AgN{O_3}$ in ammonia: Propyne’s reaction with silver nitrate in ammonia results in the formation of a white precipitate, but propene’s interaction with Tollen’s reagent produces no discernible change. This is because Tollen’s reagent undergoes a reaction when it comes into contact with acidic hydrogen, which results in the formation of a precipitate similar to what one would find in a propyne.
What kind of reaction takes place when acetylene gas is introduced to tollens’ reagent?
When ethyne is processed with Tollen’s reagent, a precipitate that is white in color is produced.
What results can be expected from the application of tollens’ reagent to acetylene?
Tollen’s reagent is well known for its interaction with aldehydes, which results in the formation of a silver mirror. Nevertheless, this reagent also reacts with a variety of other chemicals, most notably alpha-hydroxy ketones and terminal alkynes. There are a few different accounts regarding the color of the precipitate, but the most common ones are yellow, gray-white, and white.
What side effects does the treatment of acetylene with Fehling solution have?
The answer is no due to the presence of Cu2+ ions in Fehling’s solution, which do not react with acetylene. Only copper+ ions can initiate a reaction with acetylene. Because of this, it displays a red ppt.
In the presence of ammoniacal silver nitrate, which of the following produces a silver mirror?
The answer is that Tollen’s reagent is an alkaline solution that either contains an ammoniacal silver nitrate (AgNO3 + NH4OH) or a silver-ammonia complex ([Ag(NH3)2]OH).
In the presence of ammoniacal AgNO3, which does not give a silver mirror?
Tollens’ reagent is a test for determining the presence of aldehydes; it is an alkaline solution of ammoniacal silver nitrate…. Tollens’ reagent does not react with ketones in any way.
Which of the following does not have an adverse reaction when exposed to a monocle solution of silver nitrate?
Which one of the following will not react when exposed to a solution of ammoniacal silver nitrate? Because there is no hydrogen that can react acidically.
Is there a reduction of Tollen’s reagent when alkyne is used?
Tollens reagent, which is an ammoniacal silver nitrate solution, reacts with terminal alkynes to produce silver alkynides as a white precipitate, but internal alkynes do not react with Tollens reagent.
Does ethene pass the test developed by tollen?
Ethyne reacts with “Ammonical silver nitrate” and generates the desilver acetylide (white precipitate), whereas ethane does not react with the Tollens reagent. The reagents that differentiate ethane and ethyne are: a)Ammoniacal silver nitrate, which is a Tollen’s reagent:
Does C2H2 give tollen’s test?
Tollen’s reagent is also sometimes referred to as ammonical silver nitrate. In this reaction, the hydrogen that is linked to the carbon in C2H2 is acidic hydrogen. The tollens reagent then attacks the carbon that is harboring the acidic hydrogen, and it unites with that carbon to generate silver acetylide. This is the basic sequence of events that takes place.
Ammoniacal solution of cuprous chloride refers to what exactly?
A solution of cuprous chloride in ammonia might be referred to as an ammoniacal cuprous chloride solution. To make it, just combine cuprous chloride with water and ammonia and stir the mixture until the cuprous chloride dissolves and a blue-colored solution is produced. Utilizations: When ammoniacal solutions of CuCl are mixed with acetylenes, an explosive compound known as copper(I) acetylide is produced.
What are some applications for the ammoniacal reaction with cuprous chloride?
CuCl ammoniacal solutions produce complexes by absorbing carbon monoxide and reacting with it. This reaction continues to proceed to the next step, which is to dimerize the matching alkyne when oxygen is present. This reaction is the earliest known example of a homo-coupling of a terminal alkyne.
Which one of these won’t have a reaction when it’s exposed to acetylene?
Acetylene will react with strong acids such as NaOH and HCl, but it will not react with strong bases such as ammoniacal silver nitrate solution since it is a weaker acid.
What kind of reaction does the tollen test look for?
The Tollens test is a qualitative laboratory test that is used to differentiate between an aldehyde and a ketone. This test is also known as the silver-mirror test. It takes advantage of the fact that aldehydes can be easily oxidized (for more information on oxidation, check here), whereas ketones cannot.
What are the steps involved in converting acetylene to benzene?
At a temperature of 873 degrees Kelvin, benzene can be produced by heating acetylene in a tube made of red-hot iron. In the presence of extremely heated copper or iron, ethyne has the potential to be directly transformed into benzene. In this manner, one link is broken in each molecule so that it can connect to the molecule next to it in a circular form. This is how benzene is obtained directly.