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Which of the following is ortho para dir...

Which of the following is ortho para directing

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To determine which of the given groups are ortho-para directing, we need to analyze the electron-donating or electron-withdrawing nature of each substituent on the benzene ring. Here’s a step-by-step solution: ### Step 1: Understand Ortho-Para Directing Groups Ortho-para directing groups are those that increase the electron density at the ortho and para positions of the benzene ring. These groups typically have lone pairs of electrons or exhibit +I (inductive) or +M (mesomeric) effects. ### Step 2: Analyze Each Option Let’s analyze each option provided in the question: **Option 1: C=O NHCH3** - The carbonyl group (C=O) is an electron-withdrawing group. It pulls electron density away from the benzene ring, making it less nucleophilic. Therefore, this group is not ortho-para directing. **Option 2: NHCOCH3** - The nitrogen (N) in this group has a lone pair of electrons. Although it is involved in resonance with the carbonyl, it can still donate electron density to the benzene ring. Thus, this group is ortho-para directing. **Option 3: COOCH3** - The carbonyl group (C=O) here is also an electron-withdrawing group. It decreases the electron density on the benzene ring, making it less reactive towards electrophilic substitution. Therefore, this group is not ortho-para directing. **Option 4: O** - The oxygen atom has lone pairs of electrons and can donate electron density to the benzene ring. This makes it an ortho-para directing group. ### Step 3: Conclusion From the analysis: - **Ortho-para directing groups**: Option 2 (NHCOCH3) and Option 4 (O). - **Not ortho-para directing groups**: Option 1 (C=O NHCH3) and Option 3 (COOCH3). ### Final Answer The ortho-para directing groups among the options provided are **Option 2 (NHCOCH3)** and **Option 4 (O)**. ---
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In the electrophilic substituion of benzene ring, the second substituent is directed by the group already present. Electron releasing groups (+I and +M) are ortho-para-directing and activating, whreas the electron withdrawing groups (-I and -M) are meta-directing and deactivating. Halogens are placed under the category of +T (Tautomeric) groups because they have -Ibdyctuve abd +Mesomeric effect. These groups are deactivating but ortho-para-directing. In the introduction of third group to the benzene ring, the product of minimum steric gindrance is formed. Which of the following is not an ortho, para-directing group ?

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MOTION-AROMATIC COMPOUND-Exercise - 2 (Level-II)
  1. The structure of the compound that gives a tribromo derivative on trea...

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  2. Amongst the following, moderately activating groups is

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  3. Which of the following is ortho para directing

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  4. Of the species PhSH, Ph underset(O)underset("||")(S)R, ph underset(O)u...

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  5. Which of the following group(s) activate the benzene ring towards elec...

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  6. Statement-1 : Rate of nitration is C(6)H(6) cong C(6) D(6) cong C(6)T(...

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  7. Product (A) will be

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  8. Product (A) is

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  9. Which aromatic compound is obtained when noctane undergoes catalytic h...

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  10. Benzoic acid may be prepared by the oxidation of:

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  11. Isopropylbenzene can be prepared by :

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  12. In which of the following reaction t-butylbenzene is formed:

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  13. Product is

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  14. Which of the following reactions of bezene proves the presence of thre...

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  15. Electrophile NO(2)^(o+) attacks the following in which cases NO(2)^(o...

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  16. The reaction of replacement of a hydrogen atom in benzene by alkyl gro...

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  17. Which of the following statements is correct:

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  18. Which of the following gives Friedel Crafts reac- tion?

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  19. Which of the following can be used in Friedel Crafts reaction when ben...

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  20. The good method for converting benzene into n- propyl benzene is:

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