Naming Alkenes, IUPAC Nomenclature Practice, Substituent, E Z System, Cycloalkenes Organic Chemistry

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:
kzbin.info/www/bejne/r6vJlKWtf5hqoas
Optical Activity & Specific Rotation:
kzbin.info/www/bejne/mqaqqaOVjb-trNk
SN1, SN2, E1, E2 Reaction Mechanisms:
kzbin.info/www/bejne/nquQl4aOnsuDb9k
SN1, SN2, E1, E2 - Practice Test:
kzbin.info/www/bejne/p4XGY6irmZyHjLc
Alkene Reactions Review:
kzbin.info/www/bejne/ony1gItneJV9iNU
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Alkyne Reactions Review:
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Organic Chemistry PDF Worksheets:
www.video-tutor.net/orgo-chem.html
Organic Chemistry 1 Exam 2 Playlist:
bit.ly/3PKEApB
Organic Chemistry 1 Final Exam Review:
kzbin.info/www/bejne/m5uVoYaNrJuIadk
Full-Length Videos and Worksheets:
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Organic Chemistry PDF Worksheets: www.video-tutor.net/orgo-chem.html Full-Length Exams and Worksheets: www.patreon.com/MathScienceTutor/collections Alkene Reactions: kzbin.info/www/bejne/ony1gItneJV9iNU

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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?

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I also noticed that!

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The double bond needs to be included in the main root chain. @@sanyasarin

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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

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the double bond has to be included in the longest chain. It means the WHOLE bond, not just a part of it

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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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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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the compound at 2:45 can also be written as 2-methylhex-3-ene, right?

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How do you know when to write the prefix before or after? Like why is it sometimes butadiene, but its diethyl, not ethyldiene?