![Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)](https://www.bartleby.com/isbn_cover_images/9780393655551/9780393655551_smallCoverImage.gif)
Interpretation:
The mechanism for the given reaction is to be proposed.
Concept introduction:
In the nucleophilic addition reaction of nitriles, lone pair on the cyanide group acts as a nucleophile and abstracts the proton from ammonia under weak acidic condition. Next step is nucleophilic addition of ammonia group on the electrophilic carbon atom. Under the acidic condition, the electrohile becomes stronger. The protonated group acquires the partial positive charge on its electrophilic carbon atom. After all cyano groups get protonated, the cyclic intramolecular interaction between lone pair of
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 18 Solutions
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
- In general, which is more polar, the stationary phase or the mobile phase? The stationary phase is always more polar The mobile phase is always more polar It depends on our choices for both stationary and mobile phase Their polarity doesn't really matter so we never consider itarrow_forwardPlease helparrow_forwardDraw the mechanism of aspirin synthesis in an basic medium and in a neutral medium, showing the attacks and the process for the formation of the product.arrow_forward
- Na :S f. F NO2arrow_forwardQ1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. + CI OH woཡི།༠w Br H مه D CI ပ။ Br H, Br Br H₂N OMe R IN Ill N S H CI Br CI CI D OH H 1/111arrow_forwardDraw the two products of the reaction. H₂C. CH₂ H :0: CH3 CH₂ +1arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305580350/9781305580350_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305080485/9781305080485_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780618974122/9780618974122_smallCoverImage.gif)