본문으로 건너뛰기
Hub Nexus
업데이트됨

작성자아직 작성자가 없습니다맡기

개선할 점이 보이나요? 변경을 제안하세요.

후원

이 페이지는 공개 상태입니다.

매거진 Structural Biochemistry · 952개 중 68번째 페이지

Trans Esterifcation

This is an organic reaction for the preparation of esters. Instead of Fischer esterification (ester synthesis through carboxylic acid and alcohol) trans-esterification method allows R-substituent to exchange from an alcohol to the ester and vice versa. This is made possible through the use of acid or base catalysts.

Acid Catalyzed Trans-Esterification

Strong acids such as sulfuric, phosphoric, and hydrochloric acids can be used to catalyze the reaction.

Mechanism: In acidic conditions, protonation occurs at the carbonyl and enables a partial positive carbon. This is where the alcohol attaches and then deprotonated by another alcohol. The formation of a tetrahedral complex occurs and an -OR’ group will be protonated due to acidic conditions. It will leave and form a new ester with the R substituent from the alcohol.

Base Catalyzed Trans-Esterification

Bases can be used to catalyze the reaction (for example, K2CO3 or NaOH).

Mechanism: In basic conditions, deprotonation of the alcohol occurs and enables a strong nucleophile to attack the partial positive carbonyl carbon. In response to the new attachment, electrons move from the double bonded oxygen to form a negative charge on the oxygen. To stabilize the tetrahedral complex, the lone pairs of electrons reform and force the OR’ group to leave. The remaining product is an ester with a new R-substituent, and a negatively charged OR’.

Importance of Trans-Esterification

Biodiesel is an ester product that is made possible by trans-esterification. It starts out with triglyceride and excess methanol to form methyl-esters and glycerol. This process is used to make bio-fuel. However, because it is found in oils of food products, it isn’t the best way to mass-produce because of food scarcities. It is a good alternative to fossil fuel and a lot of fast food restaurants convert their cooking oil into useable bio-fuel.

References

Otera, J;Transesterification.Chem.Rev.1993. 93,1449-1470 http://pubs.acs.org/doi/pdf/10.1021/cr00020a004

"Biodiesel Synthesis." (n.d.): 1-3. Web. http://faculty.northseattle.edu/tfurutani/che238_2006/biodiesel.pdf

Where this page came from

This page was imported from Wikibooks. From “Structural Biochemistry” on Wikibooks, by its contributors, under CC BY-SA 4.0. Changed here: set as a page; navigation and edit links left out; each image under its own licence, credited in its caption.

Nobody has written it yet — it is the source material at a new address, which is why search engines are asked to skip it and why no one earns from it. It is up for grabs: take it on, and it is yours to rewrite and to earn from.

이 페이지가 속한 매거진Structural Biochemistry

언어English

이용 허락: CC BY-SA 4.0 · 출처 en.wikibooks.org

견해

코멘트

Spinner Logo
버전: 2CC0 1.0 (퍼블릭 도메인)
The runaway star that left the Tarantula Nebula
버전: 2CC0 1.0 (퍼블릭 도메인)
The Blackwell School, where segregation had no law behind it
버전: 2CC0 1.0 (퍼블릭 도메인)
The Eagle Nebula, seen in the infrared
버전: 2CC0 1.0 (퍼블릭 도메인)
The house where the Equal Rights Amendment was written
버전: 2CC0 1.0 (퍼블릭 도메인)
The Aleutians, the forgotten front of the Second World War
버전: 2CC0 1.0 (퍼블릭 도메인)
The Cosmic Cliffs are not cliffs