Recent content by proton007007

  1. P

    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 ?
  2. P

    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 .
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    Energy of Electrons: Explained

    The sign is important . Comparisons are drawn based on the algebriac value of potential energy .
  4. P

    Why reducing nature of hydrides increases down a group?

    Please provide an example where you have the doubt
  5. P

    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...
  6. P

    What is the Mechanism of Trinitration of Phenol?

    Anyway this was what I posted out there ( same question ) and got the answer . Thanks !
  7. P

    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" .
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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 .
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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 .
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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 :)
  11. P

    Equilibrium Problem: Relationship Between Q, K, and ∆G

    Its correct . change in gibbs free energy becomes zero when equilibrium is attained
  12. P

    What is the Mechanism of Trinitration of Phenol?

    And you have got the reason of toluene wrong . Its not +I effect but the hyperconjugation .
  13. P

    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 .
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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
  15. P

    What is the Mechanism of Trinitration of Phenol?

    But in that case trinitration of toluene shoulalso happen which is not correct
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