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2 votes
1 answer
435 views

Reaction of unsaturated lactone and alcohol

Image source I found this equation to turn this compound into an ketoester but I am unsure of the reaction mechanism. I postulate that the alcohol attacks the carboxyl carbon, the O becomes formally ...
bobsburger's user avatar
-1 votes
2 answers
222 views

Can a weak acid react to give a stronger acid? [closed]

I was trying to understand why $\ce{AgCl}$ does not dissolve in $\ce{HNO3}$ and the reaction I could think of was something like this: $$\ce{AgCl + HNO3->AgNO3 + HCl}$$ I could not understand why ...
Mia's user avatar
  • 11
3 votes
1 answer
786 views

Why can't Grignard reagents react like Organolithium does (with acids)?

I'd read yesterday that Grignard reagents can't give ketones on reaction with carboxylic acids. It is because of the fact that Grignard reagent is a "super-base", and it will deprotonate the ...
Rahul Verma's user avatar
  • 3,071
40 votes
6 answers
12k views

How does ammonium nitrate explode on its own?

I thought ammonium nitrate was an oxidizer that needed to be mixed with fuel to form a high explosive (e.g., ANFO). But apparently there have been accidental explosions involving just the "...
Rob N's user avatar
  • 1,633
2 votes
0 answers
55 views

Reactivity comparison between benzaldehyde and acetaldehyde [duplicate]

One of my teacher says that $\ce{Ph-CHO}$ is more reactive than $\ce{CH3-CHO}$ in performing nucleophillic addition reaction because $\ce{—Ph}$ is planar and thus offers less steric hindrance as ...
Shreyansh 's user avatar
4 votes
1 answer
3k views

Beckmann rearrangement v/s dehydration of Oximes

In the above question, A is an oxime, which is then reacted with phosphorus pentoxide. Now, phosphorus pentoxide is both a dehydrating reagent and a reagent used for Beckmenn rearrangement, but which ...
user avatar
2 votes
2 answers
840 views

Reaction between Copper nitrate and ascorbic acid

I am confused on the products of reaction between copper nitrate and ascorbic acid. When I searched this online, one of the reactions I got was: $$\ce{2Cu(NO3)2 + C6H8O6 <=> 2CuO + 4H2O + CO2}$$ ...
user510's user avatar
  • 864
4 votes
2 answers
2k views

Why are Friedel Crafts reaction not possible for molecules less activated than benzene?

I know that Friedel Crafts alkylation reaction are not possible for aniline and phenol since they form complexes with Lewis Acids. But our teacher told us that Friedel Crafts reactions aren't possible ...
Arindam Paul's user avatar
4 votes
1 answer
3k views

Reactivity of different alcohols with NaNH2 and CH3I

Identify the final product (B) in the following reaction: I'm not sure how $\ce{NaNH2}$ and $\ce{CH3I}$ will react with the different types of alcohol present here. According to my solution,ether was ...
student's user avatar
  • 105
0 votes
0 answers
204 views

Is the activation energy always inversely proportional to the reaction rate?

When I obtained the activation energy using the Arrhenius equation for a 10-minute glowstick (rapid, rigorous reaction), it was almost 4 times that of a 12-hour glowstick (slow, mild reaction). ...
Andrew Norfield's user avatar
4 votes
2 answers
389 views

When aluminium is ignited in atmosphere, will it form only aluminium oxide or also aluminium nitride?

We know when lithium is burnt in air, it forms lithium nitride and lithium oxide. I am wondering if this applies to aluminium (other metals) also?
user avatar
1 vote
1 answer
3k views

Friedel-Crafts Alkylation of Pyrrole [duplicate]

I thought that I already know how the Electrophilic Aromatic Substitution (EArs) for Aromatic rings work but then this reaction was shown to me and I was really sure that my professors didn't bothered ...
Kent de los Reyes's user avatar
1 vote
0 answers
593 views

Mechanism of Bis-decarboxylation of α,β-dicarboxylic acid

According to an internal test series in FIITJEE, it was given that the following compound decarboxylates on heating, I know that β-keto acids undergo decarboxylation on heating, but I was not sure ...
Rahul Verma's user avatar
  • 3,071
0 votes
1 answer
5k views

why lithium is less reactive than sodium? [duplicate]

Lithium lies above sodium in a group and is also smaller in size. According to periodic trend reactivity decreases from left to right in period and down the group.
Noor Fishan's user avatar
3 votes
2 answers
9k views

How to dissolve calcium sulfate fast?

I would like to dissolve $\ce{CaSO4}$ in a hardened condition (e.g. gypsum board) as fast as possible. I have seen in posts about $\ce{CaSO3}$ that vinegar and sulfamic acid are able to dissolve it. ...
Joe's user avatar
  • 33

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