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Draw resonance structures for the follow...

Draw resonance structures for the following
(i) `C_6 H_5 OH` (ii) `C_6 H_5 CHO` (iii) `C_6 H_5 - CH_(2)^(+)`

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To draw the resonance structures for the given compounds, we will follow a systematic approach for each compound. ### (i) Resonance Structures for Phenol (`C_6H_5OH`) 1. **Draw the Lewis Structure**: - Start with the structure of phenol: a benzene ring (C6H5) with a hydroxyl group (-OH) attached. - The oxygen has two lone pairs of electrons. ...
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MODERN PUBLICATION-ORGANIC CHEMISTRY: BASIC PRINCIPLES AND TECHNIQUES-(CONCEPTUAL QUESTIONS 1 )
  1. Draw structures of all isomeric ethers corresponding to molecular form...

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  2. What is the hybridisation of .each carbon in CH2 = CH -CH3 ?

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  3. Show the polarisation of carbon-magnesium bond in the following struct...

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  4. What type of structural isomerism is shown by

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  5. How many cyclic and acyclic isomers are possible for the molecular for...

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  6. In which C-C bond of CH3 CH2 CH2 Br, the inductive effect is expected ...

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  7. Draw the structures of (i) Pent-4-en-2-ol (ii) Cyclohex-2-en-1-ol

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  8. Draw the polygon formulae for all the possible structural isomers havi...

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  9. What is the type of hybridisation of each carbon in the following comp...

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  10. Which bond is more polar in the following pairs of molecules ? (a) H...

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  11. Which is expected to be more stable : O2 N CH2 CH2 O^(-) and CH3 CH2...

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  12. Write structures of various carbocations that can be obtained from 2-m...

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  13. Identify the most stable species in the following set of ions giving r...

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  14. Which of the following resonance structure for propenal is more stable...

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  15. Draw resonance structures for the following (i) C6 H5 OH (ii) C6 H5 ...

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  16. List the following carbocations in the order of decreasing stability :...

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  17. Explain why (CH3)3C^+ is more stable than CH3 CH(2)^(+) and CH(3)^(+) ...

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  18. Write resonance structures of (i) allyl carbocation (ii)

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  19. Write IUPAC name of the following:

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  20. Arrange the following free radicals in decreasing order of stability :

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