Question

2. Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, product intermediate structure and name (
0 0
Add a comment Improve this question Transcribed image text
Answer #1

Answer 1-1):-

1-12 CNucleothile) a) carbocation Intermediate] CElectophile) BY [Follow Markonikoffs (Poduct) Rule ] CNucleophile) Carbocat

(Nucleophi le) H (2°carbolatim) H BY 12 Hydnde hift Etechophile) 30 stable carbocation CMOYE Stable) BrO (Pm duct)

---------------

Answer 1-2):-

1-2) Hs Poy 20 carbocation) I (Produt)

----------------

Answer 2):-

(Elechophile) Br BY (Bi) BY (Nuclcophile) BY bromonium cation-intermedi (+B (poduct) 4r Ant-additon

Add a comment
Know the answer?
Add Answer to:
2. Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, product intermediate structure and name (please...
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
  • Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure a...

    Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved, please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride shift is possible, please consider it and show it in your reaction) 1) pent-1-ene ( or 1-methylcyclohexene) reacts with Br2

  • Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure a...

    Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. 53) Reaction of the following with HBr in electrophilic addition reactions Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride shift is possible, please consider it and show it in your reaction) yo...

  • Question: hydration of 2,3-Dimethyl-2-butene in presence of H2SO4 or H3PO4. Draw reaction mechanism using arrows. Please...

    Question: hydration of 2,3-Dimethyl-2-butene in presence of H2SO4 or H3PO4. Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved, please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride shift is possible, please consider it and show it in your reaction)

  • 21) 1-Methylcyclopentene reacts with H2O in presence of BH3, H2O2, NaOH,. Draw reaction mechanism using arrows....

    21) 1-Methylcyclopentene reacts with H2O in presence of BH3, H2O2, NaOH,. Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved, please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride shift is possible, please consider it and show it in your reaction)

  • Question: 1-Methylcyclohexene reacts with NBS and water (additional question for this question: what the full name...

    Question: 1-Methylcyclohexene reacts with NBS and water (additional question for this question: what the full name of NBS is, draw the structure of NBS) Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved, please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride...

  • Draw a structural formula for the major organic product of the following reaction:

    Draw a structural formula for the major organic product of the following reaction:Electrophilic addition of HBr to alkenes yields a bromoalkane. The reaction begins with an attack on the hydrogen of the electrophilic HBr by the electrons of the double bond to give a carbocation. This step follows Markovnikov's rule with the electrophilic H atom adding to the sp2 carbon containing the most hydrogens, leading to the formation of the most stable carbocation (1° < 2° < 3°). If possible, a...

  • Draw a structural formula for the major organic product of the reaction shown.

    Electrophilic addition of HBr to alkenes yields a bromoalkane. The reaction begins with an attack on the hydrogen of the electrophilic HBr by the electrons of the double bond to give a carbocation. This step follows Markovnikov's rule with the electrophilic H atom adding to the sp2 carbon containing the most hydrogens, leading to the formation of the most stable carbocation (1° < 2° < 3°). If possible, a 1,2-shift of either a neighboring hydride or methyl group can occur...

  • O- CHE Br CH2 H3C Hac Electrophilic addition of HBr toalkenes yields a bromoalkane. The reaction...

    Electrophilic addition of HBr to alkenes yields a bromoalkane. The reaction begins with an attack on the hydrogen of the electrophilic HBr by the electrons of the double bond to give a carbocation. This step follows Markovnikov's rule with the electrophilic H atom adding to the sp2 carbon containing the most hydrogens, leading to the formation of the most stable carbocation (1° < 2° < 3°). If possible, a 1,2-shift of either a neighboring hydride or methyl group can occur...

  • also show the mechanism and curved arrows for each mechanism 2. Predict the products for the...

    also show the mechanism and curved arrows for each mechanism 2. Predict the products for the reaction between le products for the reaction between Br, as well as Br/H, and the Alkenes listed below. rredict whether each reaction is syn- or anti-, Label the substrate, nucleophile and electrophile in each reaction. Substrate Structure Overall Reaction with Brz (with products) syn- or Overall Reaction with Bry/H20 (with products) anti- 3,3-dimethyl-1-1 butene 1-hexene styrene (phenylethene)

  • Please help with 1 & 2 A. Go through the steps of listing and labeling reactive...

    Please help with 1 & 2 A. Go through the steps of listing and labeling reactive features and analyzing the reaction between nucleophile and electrophile and resolving each reactive situation leading to the final product formation. Show stereochemistry if appropriate and relative amounts of products. (Z)-pent-2-ene with HBr 3-methylbut-1-ene with HBr and trace amounts of H2O2

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