Recent content by proton007007
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Why reducing nature of hydrides increases down a group?
If I am not mistaken , p-block is not a compound ! CO is the most common OXIDE reducing agent . Do you expect Sodium oxide to behave as a good reducing agent ?- proton007007
- Post #11
- Forum: Chemistry
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Why reducing nature of hydrides increases down a group?
As I said , give an exmple of the compound . Metallic and non-metallic oxides have different variations .- proton007007
- Post #9
- Forum: Chemistry
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Graduate Energy of Electrons: Explained
The sign is important . Comparisons are drawn based on the algebriac value of potential energy .- proton007007
- Post #2
- Forum: Electromagnetism
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Why reducing nature of hydrides increases down a group?
Please provide an example where you have the doubt- proton007007
- Post #7
- Forum: Chemistry
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What is the Mechanism of Trinitration of Phenol?
Almost all reactions are . Yes . TNT is produced by step by step nitration with increasing temperature and purity of acids . No problem . Chloro group is weakly deactivating itself . In chlorobenzene case , polynitration would be dependent on temperature to an extent but stating...- proton007007
- Post #16
- Forum: Chemistry
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What is the Mechanism of Trinitration of Phenol?
Anyway this was what I posted out there ( same question ) and got the answer . Thanks !- proton007007
- Post #14
- Forum: Chemistry
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What is the Mechanism of Trinitration of Phenol?
Of course the lone pair resonance is stronger . Thats why toluene will take harsher conditions than phenol . And I meant that by your theory , "even weakly acrivating groups will give the reaction" .- proton007007
- Post #13
- Forum: Chemistry
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Equilibrium Problem: Relationship Between Q, K, and ∆G
I don't see you mentioning your answer and your attempt above . Anyway , your answer is correct .- proton007007
- Post #8
- Forum: Chemistry
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Equilibrium Problem: Relationship Between Q, K, and ∆G
Well , giving out the answer directly won't do you good and it would (maybe) be against the forum rules . Think about Le Chateliers principle and the temperature variation of equilibrium constant . You must have surely learned this .- proton007007
- Post #6
- Forum: Chemistry
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Equilibrium Problem: Relationship Between Q, K, and ∆G
But its better to know the reason as luck and logical reasoning may not always help you . Google up Gibbs Free Energy :)- proton007007
- Post #4
- Forum: Chemistry
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Equilibrium Problem: Relationship Between Q, K, and ∆G
Its correct . change in gibbs free energy becomes zero when equilibrium is attained- proton007007
- Post #2
- Forum: Chemistry
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What is the Mechanism of Trinitration of Phenol?
And you have got the reason of toluene wrong . Its not +I effect but the hyperconjugation .- proton007007
- Post #11
- Forum: Chemistry
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What is the Mechanism of Trinitration of Phenol?
the methyl group activates o-p by HC , if nitration indirectly activates meta position , why shouldn't toluene give trinitration . Since your argument is not based on the activating group , even a weakly activating group should give the rxn .- proton007007
- Post #10
- Forum: Chemistry
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What is the Mechanism of Trinitration of Phenol?
even a weak o-p director should give trinitration but all don't give- proton007007
- Post #8
- Forum: Chemistry
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What is the Mechanism of Trinitration of Phenol?
But in that case trinitration of toluene shoulalso happen which is not correct- proton007007
- Post #7
- Forum: Chemistry