Reduction of Ketones and Aldehdyes Made Easy! - Organic Chemistry
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- Опубликовано: 12 сен 2024
- Tired of reacting with Aldehydes and Ketones? Do you want to bring them down to alcohols so that you can do easier reactions with them? If so, then it sounds like you guys need to use some reducing agents! Practice your reducing skills in this video lesson where I challenge you guys to choose the correct reducing agent and predict what your product will be when you reduce aldehydes and ketones.
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●LiAlH4 Reaction Map: upload.wikimedi...
● Bloopers: • Bloopers for Reduction...
● NaBH4 Sodium Borohydride versus LiAlH4 Lithium Aluminum Hydride: • NaBH4 and LiAlH4 Reduc...
● Wolf-Kishner Reduction Made Easy!: Coming Soon
● The Wittig Reaction Made Easy: goo.gl/eXiqQt
● Hemiacetals, Ketals, Acetals Series: goo.gl/n0fdqy
● Imines and Enamines Made Easy: goo.gl/cK4ja3
● Concepts covered/related: Hydrogenation with Patinum / Palladium / Nickel | Carbonyl Chemistry | Reduction of Carbonyl Compounds | Wolff Kishner Reduction with Hydrazine | Clemmenson Reduction | Lithium Aluminium Hydride | Sodium Borohydride | DIBAL-H | LiAl(OTBU)3H | Hydrides
●Private Tutoring Information:
I offer in-person private tutoring in Boston and NYC, and if you live elsewhere on this awesome planet I offer online Skype tutoring that is accompanied with a whiteboard program. For more info check here: orgomadeeasy.or... and contact me via my "Orgo Made Easy" Facebook page or email: OrgoMadeEasy@Gmail.com
Make sure you share this with your friends if you found it helpful, and I would love it if you leave some comments to let me know if I'm on the right track ;).
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THANK YOU FRANK!!!! I especially enjoy the explanations behind the reactions. AWESOME --- SIMPLY AMAZING FRANK
Thanks! :] Really appreciate the awesome feedback from you guys! Hope you did well on your exams.
I subscribed as soon as I saw the intro! Looking forward to these videos. 😂😂😂
😂👍🏼 welcome to Orgo Made Easy!
why at the end of semester i found this channel , if i would find it earlier my grade would be good, thanks man u are so great at explaining
You guys are so awesome! I love the new intros, and the cool seque clip! Thanks for another great video. I don't know how you do it!!
Thanks Drew! Really appreciate the support from you. :] I'm currently working on the mechanism video+bloopers so keep an eye out. haha
Thank you very much.you make this easier for me 😊😊
You are so good, I love all of your videos! Thanks so much!
Beckkkahhhx3 Thanks for the feedback Becka! :] It's because of students like you give me all the motivation to keep going at it. :D
Really I smile when watch your video
you make the Organic Chemistry more easy
Thanks ^^
Lama Al-Ahmadi Haha thanks Lama! That's awesome to hear. :] I'm glad my vid. could do that for you. Gluck studying!
Is there like some sort of homework or practice problems i can do to help supplement learning? Im suppose to be a chem major but i dropped a nice C on o chem 1 :/ and i really want the A on o chem 2.
ShotClanTxter Sorry to hear, but I'm sure you can do it. I went from a B to an A and I've had students start off with a F in Orgo I and end with an A-. ;) Here are some problems, with solutions. You need to scroll down to the reduction portion of the article. :] www2.chemistry.msu.edu/faculty/reusch/virttxtjml/aldket1.htm
Great video! Thank you
MissSharon95 Your welcome! I'm glad you liked it. :D
can u please do video on the preparation of aldehydes and ketone from esters?
Hey! Can't we use DIBAL-H for this kind of reduction? It Also preserves the unsaturation in the Alkane, right?
Hey Hardik I'm not sure actually but the only time I've seen DIBAL-H is for reducing Esters to Aldehydes so it makes me think DIBAL-H wouldn't reduce the Aldehyde nor Alkene. Another unique reagent that's good to keep in mind is LiAl(OTBu)3-H which is extremely similar to DIBAL-H in that it can convert a Acyl Chloride into an Aldehyde.
You're awesome. Keep going.
+Nikki Lim I'm going I'm going! lol In the meantime if you want other great resources for Orgo make sure you know about these guys/gals ruclips.net/video/1QkGxQCI1es/видео.html
can we reduce carboxylic acid to make ketone
Tejas Bhukal Hmm off the top of my mind I don’t think you can do it in one step. If you treat Carb Acid w SOCl2 and turn it into an Acid Chloride and then treat it with 1 Equiv of a Gilman Reagant ie (CH3-Cu-CH3) you can attack the carbonyl with a CH3 and kick off the Cl. And end up with a Ketone with CH3 as one of its R groups.
@@OrgoMadeEasy thank you sir for your answer.
i got it what you wanted to say of show . thanks again
@@OrgoMadeEasy what's gilman reagant
I don't like your choice of example compounds. The products of the sodium borohydride reduction will tautomerize back to a ketone and aldehyde.
You are the best!
Thanks Thed! Glad these vids are still coming in handy 😊!
Happy Studying! 💪🏼
REDUCING AGENT DEFINITION MADE EASY !!
Im depending on these videos to get me into university...
Frank you my angel... bless you x 24578887 millions times ... te amo
tks so much. can i follow you ?
your exm very easy
Of course you can Trinh. :] Thanks for watching! You can subscribe via RUclips to my channel and if you have a facebook just look up "Orgo Made Easy" and you should be able to find my facebook page.
awesome
Are you Korean ??
which is the other reducing agent that reduces both alkene and the double bond in acids
sorry
I meant to alkene and ketone /aldehyde
I don't want to preserve the alkene and reduce both then which reducing agent should I use?
+hiten shah H2, Pt or H2, Ni both should do the trick :]
+Frank Wong Thanks :)
You can use Sn-HCl.
so good