In organic chemistry, ring strain is a type of instability that exists when bonds in a molecule form Adolf von Baeyer received a Nobel Prize in for the discovery of the Baeyer strain theory, which was an explanation of the relative stabilities. Sachse Mohr’s theory (Theory of strainless rings). ❖ Baeyer’s Strain Theory. – Baeyer postulated that any deviation of bond angles from the normal tetrahedral . Baeyer Strain Theory. In , Adolf von Baeyer published a paper on polyacetylene compounds in the journal of the German Chemical Society. At the end of.

Author: Zololkree Mogis
Country: Zambia
Language: English (Spanish)
Genre: Education
Published (Last): 26 November 2012
Pages: 188
PDF File Size: 7.15 Mb
ePub File Size: 2.39 Mb
ISBN: 688-8-50673-571-9
Downloads: 51743
Price: Free* [*Free Regsitration Required]
Uploader: Feramar

Please try again later.

Learn More in these related Britannica articles: The awkward case of ‘his or her’. Unfortunately, our editorial approach may not be able to accommodate all contributions. The potential energy and unique bonding structure contained in the bonds of molecules sfrain ring strain can be used to drive reactions in organic synthesis.

And is one way more correct than the others? Retrieved from ” https: Please note that our editors may make some formatting changes or correct spelling or grammatical errors, and may also contact you if any clarifications are needed.


In cycloalkanes, each carbon is bonded nonpolar covalently to two carbons sttain two hydrogen.

A quantitative measure for angle strain is strain energy. Views Read Edit View history. Other cycloalkanes that do not have 3- and 4-membered rings can be strained.

Strain theory

Get Word of the Day daily email! Keep Exploring Britannica Photosynthesis. In organic chemistryring strain is a type of instability that exists when bonds in a molecule form angles that are abnormal.

These include cyclophanes stain, Platonic hydrocarbonspyramidal alkenesand cyclic alkynes.

Angle strain also is the basis of Bredt’s rule which dictates that bridgehead carbon centers are not incorporated in alkenes because the resulting alkene would be subject to extreme angle strain. Take the quiz Naughty or Nice Quiz He’s making a quiz, and checking it twice What is the internal angle of a regular pentagon or hexagon?

Angle strain destabilizes a molecule, as manifested in higher reactivity and elevated heat of combustion.

Angle strain occurs when bond angles deviate from the ideal bond angles to achieve maximum bond strength in a specific chemical conformation. Do the calculation for each of these cyclic hydrocarbons. The value for cyclobutane should be 9 o 44′. Illustrative is C 60 where the carbon centres baeyed pyramidalized.

Ring strain

Have your cake and eat pie too. Time Traveler for Bae yer strain theory The first known use of Bae yer strain theory was in See more words from the same year. Thus, baeer should be an axial cyclohexanecarboxylic acid and an equatorial one. Internet URLs are the best. At strin end of the paper, a discussion appeared on the strain in small baeyfr compounds.


If you prefer to suggest your own revision of the article, you can go to edit mode requires login. There was a problem with your submission. Our editors will review what you’ve submitted, and if it meets our criteria, we’ll add it to the article.

Test Your Knowledge – and learn some interesting things along the way. Comments on Bae yer strain theory.

Strain theory | chemistry |

Comments on Bae yer strain theory What made you want to look up Bae yer strain theory? Angle strain and torsional strain combine to create ring strain that affects cyclic molecules. The carbons have sp 3 hybrization and should have ideal bond angles of Literally How to use a word that literally drives some people nuts.