Answer the following questions on the basis of final product. (Refer Image)
Let,
●Degree of unsaturation be X.
● No. Of rings be Y.
●No. Of distinct products it gives on reductive ozonolysis be Z.
●Assign
A=1 (For Aromatic Product)
A=2 (For Non Aromatic Product)
A=3 (For Anti Aromatic Product)
Find the value of
( X + Y + Z + A ) Z − A
Clarifications
●All steps of reaction will occur.
●In steps E-F and H-I the reaction must be done as much as possible.
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@Aaron Jerry Ninan , is it okay?
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Yes......correct!!!! ( you can also explain how you got no. of ozonolysis products, as most people will get that wrong)
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Arre, thik hai.. And how are my reposts today?
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@Md Zuhair – Good....(even though they were not new questions)
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@Aaron Jerry Ninan – New in the sense? New to you, or new in brilliant?
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@Md Zuhair – New to me.
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@Aaron Jerry Ninan – Oh, the concepts were old and were done by you, you meant? What can i do, I just reposted the questions I did. Hehe
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@Md Zuhair – Please find some good problems for PNC
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@Aaron Jerry Ninan – There are many, Try Aniket's Set, Waise, can you come to whatsapp for a bit, need to talk
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@Md Zuhair – I dont have phone with me right now
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@Aaron Jerry Ninan – Okay, In this question https://brilliant.org/problems/hurry-up-its-jee-today/?ref_id=1480345 , The grids which are only boxed are the paths na? And also tell, that how do we put condition such that it doesnt passes through M?
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@Md Zuhair – Yes.....exclude that from total that passes through M
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@Aaron Jerry Ninan – Total passes, Wouldnt that be quite lenghty, Idk, i am just saying it without trying. Tell me if it will
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@Md Zuhair – No.....you can get that very fast using appropriate pnc concepts
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@Aaron Jerry Ninan – Okay! Lets see that!
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@Md Zuhair – Sorry , but what are the products of ozonolysis of napthalene ? @Aaron Jerry Ninan @Md Zuhair Thanks !
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@Winston Cahya – Actually I don't remember the products. But try using resonance in the structure and then apply ozonolysis for the two different products of resonance. You will get 3 diff. Products in ozonolysis
wont the ring be affected in formation of D? https://chemistry.stackexchange.com/questions/10653/why-does-cyclopropane-react-with-bromine
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No it wont, as it will get 3 degree position which is most stable
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