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Naming Alkenes, IUPAC Nomenclature Practice, Substituent, E Z System, Cycloalkenes Organic Chemistry
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- Опубликовано: 6 авг 2024
- This organic chemistry video explains how to name alkenes using the iupac nomenclature system. It contains examples with substituents, cycloalkenes, cis trans isomers and naming alkenes using the e z system.
Stereochemistry R/S Configuration:
• Stereochemistry - R S ...
Optical Activity & Specific Rotation:
• Optical Activity - Spe...
SN1, SN2, E1, E2 Reaction Mechanisms:
• SN2 SN1 E1 E2 Reaction...
SN1, SN2, E1, E2 - Practice Test:
• SN1 SN2 E1 E2 Reaction...
Alkene Reactions Review:
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Organic Chemistry 1 Exam 2 Playlist:
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Organic Chemistry 1 Final Exam Review:
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Alkene Reactions: ruclips.net/video/lKROX1C0JRs/видео.html
Students watching in 2024
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Cramming for my orgo exam and was confused on the z and e configuration with more than one double bond and you explained it perfectly. Thanks a lot man you are a blessing!
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At 8:22 couldn't you have started at the very left with 1 and counted 3 as the double bond, making the longest strand 8?
I also noticed that!
The double bond needs to be included in the main root chain. @@sanyasarin
No, you have to include both the carbons involved in the double bond, in the configuration you suggested only one of the carbons involved in the double bond is considered. @@sanyasarin
the double bond has to be included in the longest chain. It means the WHOLE bond, not just a part of it
the double bond needs to have the lowest number which is 1 so the chain starts from there
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its 2 a.m. watching videos of how to name Alkanes, Alcohols, Alkenes, Alkyne, Cyclic structures, and Aromatics and you simplify this so much, thank you.
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7:48 It's always good to remember that the chain has to go through the double-bond, even if you could make a longer chain elsewhere. Thanks for the explanation and all of the examples!
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8:10 why is the chain only 7? You can start counting on the left most carbon to make it 8.
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Pretty good, but you should have included some double bond chains outside of a ring with double bonds inside. You helped get some big concepts though, good job!
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Very good Explanation
how do you determine E or Z if one side has a cyclohexane attached to the carbon double bond??
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I'm wondering about the reverse exercise, namely being given a longish IUPAC name and being required to draw the molecule.
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Right. At first I'm like oh easy, double bonds means end everything with ene ... then came the addition of other molecules being attached which made it even more confusing as well as multiple double bonds turning it into diene, triene, etc and having to put it all in alphabetical order 😭
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the compound at 2:45 can also be written as 2-methylhex-3-ene, right?
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I had a question that how can alkenes have 2 double bonds as it won’t satisfy the C2H2 rule
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For the example at 8:33, isn't the priority to find the longest chain? As such, shouldn't the left ethyl group be part of the chain, and the double-bond be called a 2 methyl groups?
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