Question

4 15. React the following with HNO:/H,SO, and show the final substituted benzene product. On the line provided state if the reaction was Electrophilic aromatic substitution of Nucleophilic aromatic substitution HNO H,SO, HNO,/H,S0 HNOyHSO, HNO HSo HNO,/H,SO NNOyH.SO 0% CH,ONa ?,o ether

0 0
Add a comment Improve this question Transcribed image text
Know the answer?
Add Answer to:
4 15. React the following with HNO:/H,SO, and show the final substituted benzene product. On the...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • What is the product of the 1 но reaction? so NO 6. What is the product...

    What is the product of the 1 но reaction? so NO 6. What is the product of the reaction он HSO (B) (A) NO он NO HOS (B) (A) soH (D) (C) NOz OH HO. both (B) and (C) (D) (C) HO,S 2 What is the product of the reaction? NoOH Which compound will yield only one product after nitration with HNO/HSo 7. OH .сн, (A) (B) сHа- (B) (A) но,, сн, OH (C) (D) сH,сH, none of the these...

  • Help with these! ( H 7. Acyl Substitution Practice. Show the first couple of mechanistic steps...

    Help with these! ( H 7. Acyl Substitution Practice. Show the first couple of mechanistic steps in a Fischer Esterification. Show the final product h︿cu2 wheu . (3) (a) show first intermediate using H+ 해 ..0-CH2CH3 (b) show intermediate after electrophile & nucleophile bond (c) draw final product (More steps) a. Identify (circle and label). (4) the nucleophilic atom, electrophilic atom, and leaving group in the reaction below 0 b. Why is the reaction above expected to go faster than...

  • Add the following questions to the final report: a) Why does the carbomethoxy group directs the...

    Add the following questions to the final report: a) Why does the carbomethoxy group directs the reaction to positions that are meta to it? b) Why the formation of dinitrobenzaote is substantially disfavored ? c) Would you expect small amounts of the ortho and para substituted product? How would you remove them if they are formed ? d) Why does water have a retarding effect on the nitration ? e) Explain why Benzene has lower reactivity in electrophilic addition reactions...

  • which products would be obtained by 40. Select he best synthesis of Which of the following...

    which products would be obtained by 40. Select he best synthesis of Which of the following compounds will not undergo nucleophilic aromatic substitution? 44. a. 1-chioro-2,4 dinitrobenzene сснз m-chloronitrobenzene (CHshCCI CH,CCI 41. Provide the reagentís) necessary to AICI3 oluene to AICI, benzoic acid. b. NBS, heat d.1.COz 2, но. Provide the structure of the major product(s) for the CH CCI AICİ3 Benzene b) AICI 3 42. (CH3)2C CH2 HF following reaction. Benzene AICly 45. Which of the following would be...

  • Aromatic substitution Give the major product of the following reaction. HNO, OH HSC HC Give the...

    Aromatic substitution Give the major product of the following reaction. HNO, OH HSC HC Give the major product of the following reaction: HASA Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene. Give the major product of the following reaction. Give the major product of the following reaction. Draw the starting material if no reaction occurs. Give the major product of the following reaction. Draw the starting material if no reaction occurs. NO 2 Give the major product of...

  • D Question 11 6 pts Which structure is a major organic product of the multi-step reaction...

    D Question 11 6 pts Which structure is a major organic product of the multi-step reaction shown? Recall that the numbers in front of the reagents tells the order of the addition 1) NaNHANH, 2) CH CH Br 3) HgSO4/H2SO4/H,0 // D Question 14 6 pts Which group is considered a deactivator in electrophilic aromatic substitution (EA.S.) reactions? The dashed line indicates where the group is attached to benzene. OH —ОН

  • 9:09 AM Mon Apr 29 ゃしダ46% ■ f) What is the major organic product obtained from the following reaction? CrOs он HSO,, H20 1-butene, CH,CH,CH CH butanal, CH CH.CH,CHO CH,CH,COCH butanoic acid, C...

    9:09 AM Mon Apr 29 ゃしダ46% ■ f) What is the major organic product obtained from the following reaction? CrOs он HSO,, H20 1-butene, CH,CH,CH CH butanal, CH CH.CH,CHO CH,CH,COCH butanoic acid, CH,CH,CH,COO g) In electrophilic aromatic substitution reactions a bromine substituent A) is a deactivator and a m-director. B) is a deactivator and an o,p-director. C) is an activator and a m-director D) is an activator and an o,p-director E) none of the above h) In electrophilic aromatic substitution...

  • 1) What is/are the product (s) in the following reaction so,0, A) I only B) Il...

    1) What is/are the product (s) in the following reaction so,0, A) I only B) Il only C) III only D) II and IV E) I and IV 2) A -NO2 substituent on the aromatic ring is a _in electrophilic aromatic substitution reactions. A) a deactivator and a m-director. B) a deactivator and an o,p-director. C) an activator and a m-director. D) an activator and an o,p-director. 3) Which compound would be expected to show a broad peak around 3000cm-1?...

  • Ch 15. 3 Gve the major products) of the following reaction to HNO, (1 mole) H,...

    Ch 15. 3 Gve the major products) of the following reaction to HNO, (1 mole) H, SO, heat ?? -NO ON to NO G O=0 S-OH 0 O 0-0 $-OH o + OH There is no reaction under these conditions of the correct product is not listed here o=o=0 OH HOP ON S-OH O NO NO There is no reaction under these conditions, or the correct product is not listed here 10%3D%3D0 -OH Gve the major product(s) of the following...

  • 1.The main product of the reaction between p-cresol and Br2 / FeBr3 is: 3-Bromo-4-methyl phenol 2-Bromo-4-methyl...

    1.The main product of the reaction between p-cresol and Br2 / FeBr3 is: 3-Bromo-4-methyl phenol 2-Bromo-4-methyl phenol 2-methyl-4-bromine phenol 3-methyl-4-bromine phenol 2.Which of the following compounds is the least reactive in the nucleophilic substitution with NaOH? 2,4-dinitrochlorobenzene m-nitrochlorobenzene o-nitrochlorobenzene 3,5-dinitrochlorobenzene 3.What is the mechanism (s) for the reaction of 4-bromo-1-nitrobenzene with sodium hydroxide to form 4-nitrophenol? bimolecular nucleophilic substitution (Sn2) aromatic nucleophilic substitution by addition-elimination aromatic nucleophilic substitution by elimination-addition aromatic electrophilic substitution 4.which of the following is the correct...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT