DMF/NaOH/H2O: a metal-free system for efficient and chemoselective reduction of α-ketoamides - Organic Chemistry Frontiers (RSC Publishing)
![Intramolecular Aldol Reaction Mechanism | Organic chemistry books, Organic chemistry, Science chemistry Intramolecular Aldol Reaction Mechanism | Organic chemistry books, Organic chemistry, Science chemistry](https://i.pinimg.com/736x/d0/ab/64/d0ab641297fc3ba713366c3c14aa85dd.jpg)
Intramolecular Aldol Reaction Mechanism | Organic chemistry books, Organic chemistry, Science chemistry
Advanced Organic Chemistry: Reaction Mechanism, Strategy, Applications.... - Advanced Organic Chemistry: Reaction Mechanism, Strategy, Applications.
![Propose a detailed arrow-pushing mechanism for the reaction below. [{Image src='reaction7322844887529244725.jpg' alt='' caption=''}] | Homework.Study.com Propose a detailed arrow-pushing mechanism for the reaction below. [{Image src='reaction7322844887529244725.jpg' alt='' caption=''}] | Homework.Study.com](https://homework.study.com/cimages/multimages/16/reaction7322844887529244725.jpg)
Propose a detailed arrow-pushing mechanism for the reaction below. [{Image src='reaction7322844887529244725.jpg' alt='' caption=''}] | Homework.Study.com
![SOLVED: Organic chemistry! Complete the mechanism for the following reaction. Please use structure! Complete the mechanism for the following reaction NaOH .CHO Ph H2O SOLVED: Organic chemistry! Complete the mechanism for the following reaction. Please use structure! Complete the mechanism for the following reaction NaOH .CHO Ph H2O](https://cdn.numerade.com/ask_images/5968fe163bcc4f878eef9628409c270e.jpg)
SOLVED: Organic chemistry! Complete the mechanism for the following reaction. Please use structure! Complete the mechanism for the following reaction NaOH .CHO Ph H2O
![SOLVED: The amide shown below gives different products depending on whether it reacts with bromine and NaOH/H2O or bromine and NaOMe/MeOH. Explain (hint: write the reaction mechanism): Br2, NaOH; H2O NH2 NH2 SOLVED: The amide shown below gives different products depending on whether it reacts with bromine and NaOH/H2O or bromine and NaOMe/MeOH. Explain (hint: write the reaction mechanism): Br2, NaOH; H2O NH2 NH2](https://cdn.numerade.com/ask_images/2c860fb8cf374a19ae50ce98a05dcd9f.jpg)
SOLVED: The amide shown below gives different products depending on whether it reacts with bromine and NaOH/H2O or bromine and NaOMe/MeOH. Explain (hint: write the reaction mechanism): Br2, NaOH; H2O NH2 NH2
![Organic Chemistry: Reaction Mechanism] I am just trying to determine the type of reactions the following five are so I can create a mechanism for each one. If you could tell me Organic Chemistry: Reaction Mechanism] I am just trying to determine the type of reactions the following five are so I can create a mechanism for each one. If you could tell me](https://preview.redd.it/88pxre200un61.png?auto=webp&s=337110bbbe9da003b6c4adaa67d74ca449f6822a)
Organic Chemistry: Reaction Mechanism] I am just trying to determine the type of reactions the following five are so I can create a mechanism for each one. If you could tell me
![I still don't understand why NaOH is used here in this crossed aldol reaction. For ketones, shouldnt we use LDA for reversible deprotonation? Even with a hindered substrate, wouldn't deprotonation with NaOH I still don't understand why NaOH is used here in this crossed aldol reaction. For ketones, shouldnt we use LDA for reversible deprotonation? Even with a hindered substrate, wouldn't deprotonation with NaOH](https://preview.redd.it/zx1njs8tafr81.png?auto=webp&s=ffc6c0678db008ece4014c3cf120cbd72dc67a97)
I still don't understand why NaOH is used here in this crossed aldol reaction. For ketones, shouldnt we use LDA for reversible deprotonation? Even with a hindered substrate, wouldn't deprotonation with NaOH
![SOLVED: What is the major organic product obtained from the following reaction? OH NaOH Ho OCH; 2 H;o* OH Oa 1 0b.2 c. 3 d.4 SOLVED: What is the major organic product obtained from the following reaction? OH NaOH Ho OCH; 2 H;o* OH Oa 1 0b.2 c. 3 d.4](https://cdn.numerade.com/ask_images/855058ed581e45879801d5ce057c865a.jpg)
SOLVED: What is the major organic product obtained from the following reaction? OH NaOH Ho OCH; 2 H;o* OH Oa 1 0b.2 c. 3 d.4
![Show mechanism for the reaction b. C.[{Image src='img64571650848670812494.jpg' alt='' caption=''}]omplete, show the mechanism NaOH, heat NaOH, heat H20 | Homework.Study.com Show mechanism for the reaction b. C.[{Image src='img64571650848670812494.jpg' alt='' caption=''}]omplete, show the mechanism NaOH, heat NaOH, heat H20 | Homework.Study.com](https://homework.study.com/cimages/multimages/16/screen_shot_2019-10-06_at_10.21.36_pm7883685496230764858.png)
Show mechanism for the reaction b. C.[{Image src='img64571650848670812494.jpg' alt='' caption=''}]omplete, show the mechanism NaOH, heat NaOH, heat H20 | Homework.Study.com
![For syn dihydroxylation, what is the difference between using these reagents? When would you use KMnO4/NaOH vs OsO4/NaHSO3 H2O? : r/ OrganicChemistry For syn dihydroxylation, what is the difference between using these reagents? When would you use KMnO4/NaOH vs OsO4/NaHSO3 H2O? : r/ OrganicChemistry](https://preview.redd.it/n8sxg0h00v281.jpg?width=640&crop=smart&auto=webp&s=34f34a69489c0ed25ef3a9648da7b0a252701573)