Organic Chemistry Drawing Structures - Bond Line, Skeletal, and Condensed Structural Formulas

This organic chemistry video tutorial shows you how to draw lewis structures, bond line structures and skeletal structures including condensed structural formulas. It also shows you how to draw the lewis structures of functional groups such as alkanes, alkenes, alkynes, carboxylic acids, alcohols, ethers, esters, ketones, aldehydes, amides, nitriles, and amines. This video also helps you to draw cyclic structures as well cis and trans isomers. In addition, it helps you to easily identify substituents such as isopropyl, sec-butyl, isobutyl, isopentyl, and tert butyl as well as amino, hydroxy, ethoxy, methoxy, and oxo substituents.
Organic Chemistry - Basic Introduction:
• Organic Chemistry - Ba...
Which Bond Is More Polar?
• Which Bond Is More Polar?
How To Draw Lewis Structures:
• Organic Chemistry - Ho...
Condensed Structures to Skeletal Structures:
• Condensed Structures t...
Functional Groups Review:
• Functional Groups
Primary, Secondary, & Tertiary Functional Groups:
• Functional Groups - Pr...
_________________________________
How To Calculate Formal Charge:
• Formal Charge
Finding Lone Pairs Using Formal Charge:
• How To Identify The Nu...
Dipole Moment & Electronegativity:
• Dipole Moment, Vectors...
Predicting Bond Angles:
• Predicting Bond Angles
Valence Bond Theory:
• Valence Bond Theory & ...
Hybridization of Atomic Orbitals:
• Hybridization of Atomi...
_______________________________
Bond Strength and Bond Length:
• Bond Strength and Bond...
Orbital Overlap and Bond Length:
• Hybridization, Orbital...
Organic Chemistry PDF Worksheets:
www.video-tutor.net/orgo-chem...
Organic Chemistry Exam 1 Playlist:
bit.ly/3kJnNXU
Full-Length Videos and Worksheets:
/ collections

[@TheOrganicChemistryTutor]

Organic Chemistry PDF Worksheets: www.video-tutor.net/orgo-chem.html
Full-Length Exams and Worksheets: www.patreon.com/MathScienceTutor/collections
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last example, "1-hydroxy-3-dedoxy-3-thriceoxy-4-quatroxy-x-zebroxodic acid"

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CH3-O-CH3
How lovely are thy branches

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for acetic acid , why are both oxygens attached to the carbon ? without looking at your solution i would have drawn one oxygen triple bound to carbon and the other OH bound to the oxygen, thats how i figured from the condesned formula. Or ist that not favoured because of the electronegativity of the oxygens ? 12:40

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for ethene, why are the C-H bonds drawn diagonally, instead of straight?

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@5:55 what is the molecular formula?

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[@w.balazs6424]

At 24:02 you say it's sec-butyl because it's connected to a previously secoundary carbon. My quesstion is if the long chain connects to the other secoundary carbon ( right next to the carbon where you drawed the conection in the video) whould it have the same name ? Because it is a structuraly different molecule.

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[@tag_of_frank]

For acetic acid, from the condensed formula, how can one know, if one didn't know beforehand, that we don't have CH3-C-O=OH ? Or
CH3-C=O-OH?

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oxygen only had two bonds, your first oxygen has triple bonds which is incorrect

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[@tag_of_frank]

For acetic acid, from the condensed formula, how can one know, if one didn't know beforehand, that we don't have CH3-C-O=OH ? Or
CH3-C=O-OH?
How can you tell CH3COOCH3 does not have a single bond to O, O, CH3, and Ch3?

[@athar_adv]

You can figure it out by figuring it out how many bonds atoms like to form and the maximum of how they can form
CH3 bonds to a C atom, the carbon in the metyhl group is satisfied with 4 bonds (3 hydrogen 1 carbon).
The next carbon is single bonded to the ester substituent with a single bond because that oxygen is bonded to another oxygen wich is bonded to a hydrogen (so both oxygen have 2 bonds and wont make anymore, and the hydrogen is also satisfied).

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There will be no double bonds in methyl ethanoate because all atoms are satisfied with their bonds

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