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Animations of Organic Reactions

Animations of Organic Reactions

Animations of organic reactions
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Material Type:
Animation
Date Added to MERLOT:
July 1, 2003
Date Modified in MERLOT:
September 25, 2019
Author:
 
Submitter:
Grigoriy Sereda
Primary Audience:
High School, College General Ed, Graduate School
Technical Format:
Website
Mobile Compatibility:
Not specified at this time
Technical Requirements:
A browser
Language:
English
Cost Involved:
No
Source Code Available:
Yes
Accessibility Information Available:
No
Creative Commons:
No

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Comments

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Grigoriy Sereda
Grigoriy Sereda (Faculty)
4 years ago
I have addressed you concerns and added explanations to each reaction mechanism. Enjoy!
Used in course? Yes
Liliana Soledad Rivera lersundi
Liliana Soledad Rivera lersundi (Faculty)
7 years ago

Me parece un material pertinente para ser utilizado en el aula. Creo que proporciona un buen apoyo didactico para la clase, desde un punto de vista visual, es fácil de utilizar. Sin embargo creo que podría ser mejorado incorporando un texto expicativo para cada tipo de reacción

Grace Winschel
Grace Winschel (Consultant)
8 years ago

The website provides mechanisms for some basic transformations in organic chemistry.

Technical Remarks:

The website doesn't seem to do a good job at differentiating between mechanistic steps and transition states. Bonds are shown moving with double headed arrows, and then, a transition state of bonds breaking and bonds being made is shown. This provides for repetative steps and also leads me to believe students may get confused as to what truly constitutes as a mechanistic step. Some type of differentiation would be appreciated. Also, this is quite a short list of reactions. A more thorough database of reaction mechanisms would be a large improvement.

Time spent reviewing site: 20
Ehren Bucholtz
Ehren Bucholtz (Faculty)
9 years ago
The animations would greatly benefit from either a voiced over narrative, or a side text block that explains some of the important aspects of the stereochemistry of reactions. For example, in the SN2 reaction, there is indication of 3 different R groups, but no indication as to inversion of configuration. This is also the case with regiochemistry of the epoxide ring opening reactions. For a student just learning these reactions, there is not a readily apparent reason why bases attack the less substituted carbon and under acid conditions the nucleophile comes in at the more substituted carbon. One other aspect of the acid ring opening that can be confusing it the statement that enantiomers can be formed. It would be very beneficial to have two different colored arrows showing attack of the carbocation from top or bottom and the resultant enantiomeric products in similar colors. I also think the SN1 could be improved by reversing the first and second slide in the sequence. By showing partial charges on the bromine and carbon in the initial slide, it would help students to understand why the bromine leaves and give a reason for the curved arrow. One other aspect lacking is lone pairs of electrons.

Technical Remarks:

The animations played smoothly and did not have any problems. There could be an explanation of the green button can be used to show the entire mechanism without pausing between slides.
Time spent reviewing site: 20 minutes
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