Professor Davis uses ethane to demonstrate how Newman projections are created and why they contain useful information which is not available from other structural representations.
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Yes, Rohit. I will work on something covering staggered and eclipsed conformations this week (I am also working on another video based on your earlier question on enantiomers). You are a good customer... keep coming back, please!
Not sure if I completely understand your questions, but if by 'first', you mean pointing up, then no, the order of substituents as you go around each ring only matters to the extent that you preserve the stereochemistry of each carbon. Remember that whole molecules can translate and rotate without changing their identity.
Actually, the dihedral angles are 60 degrees in the staggered conformation. Remember that dihedral angles are the angles between two bonds, one on the FRONT atom and one on the BACK atom, when the sighting along the central carbon-carbon bond.
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Thank YOU so much! I love that these videos are still helping students years later. Please remember to share and subscribe to keep my channel going!
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Wow this channel is a hidden gem and the most clear-cut easy to understand tutorial! Bravo your awesome!! Keep up the good work, I'm recommending your channel to my friends!
Very good explanation. simply the best I've heard.
Thank you!
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Simple and clear analysis! Thanks a lot
+kunle alaafia Thanks! Glad you liked it!
Very good and simple explanation. Thank you so much
+Gugu Ngwenya My pleasure. Glad it helped!
Yes, Rohit. I will work on something covering staggered and eclipsed conformations this week (I am also working on another video based on your earlier question on enantiomers). You are a good customer... keep coming back, please!
Simply amazing.....
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I'm glad you found it useful! Thanks for watching and don't forget to subscribe!
Sir.... How you rotate the individual carbon atom.... Like this... Kindly told me... You are using which application for this...
Amazing and perfect, thanks a lot.
awesome work . i owe to you a lot . could you please explain the staggered eclipsed stabilty and thier exceptions please.
Nice and helpful video.
What app are u using for editing
Thanks for the comment! For this video I used a combination of CambridgeSoft's Chem3D, MS PowerPoint and Sony Movie Studio Platinum.
ChemSurvival thanks
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In the first central carbon in the Newman projection. Does it matter which substituents you put first.
Not sure if I completely understand your questions, but if by 'first', you mean pointing up, then no, the order of substituents as you go around each ring only matters to the extent that you preserve the stereochemistry of each carbon. Remember that whole molecules can translate and rotate without changing their identity.
Thank you sooo much
very useful. thank you
great explanation
Awesome explained
Thanks!
Seeing this in 2020
sir the dihedral angle is 120 not 60.....hope am right???
Actually, the dihedral angles are 60 degrees in the staggered conformation. Remember that dihedral angles are the angles between two bonds, one on the FRONT atom and one on the BACK atom, when the sighting along the central carbon-carbon bond.
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kekul is also known as structural formula!
Nice .thanks
Wonderful
Thanks! Glad you found it useful!
informative