Anyone have a good example of an ester

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SUMMARY

This discussion focuses on the synthesis of esters, specifically the reaction between isomyl and acetate. The participants highlight the aromatic properties of esters compared to their carboxylic acid precursors, noting that esters often have pleasant smells while their counterparts can be unpleasant. A common undergraduate organic chemistry experiment involves esterifying butyric acid to produce a more fragrant compound. The conversation also touches on the challenges faced during laboratory experiments, including unexpected results.

PREREQUISITES
  • Understanding of organic chemistry principles
  • Familiarity with esterification reactions
  • Knowledge of functional groups, specifically carboxylic acids and alcohols
  • Experience with laboratory techniques in organic chemistry
NEXT STEPS
  • Research the mechanism of esterification reactions
  • Learn about the properties and applications of esters in various industries
  • Explore the use of different alcohols and acids in ester synthesis
  • Investigate common laboratory techniques for isolating and purifying esters
USEFUL FOR

Chemistry students, organic chemists, and anyone interested in the synthesis and applications of esters in both academic and industrial contexts.

afcwestwarrior
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i need help on figuring out how to combine the compounds and make them an ester, in other words i need help with esters,
 
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check this out, say i have isomyl and i make it react with acetate, how will it look and what do i do to combine them and how do i write them out
 
thanks man big time
 
I'm sure you already know plenty of examples of esters. Things that smell nice are a lot of times esters. Their carboxylic acid counterparts stink to high heaven though! A classic undergrad O chem experiment is taking something horrible like butyric acid and esterfying it to get something that smells nice.
 
gravenewworld said:
I'm sure you already know plenty of examples of esters. Things that smell nice are a lot of times esters. Their carboxylic acid counterparts stink to high heaven though! A classic undergrad O chem experiment is taking something horrible like butyric acid and esterfying it to get something that smells nice.

Heh, we just did that lab in my ochem class. Unfortunately the product was an ugly solid that smelled 10 times as bad as the goat smelling caproic acid to begin with. Got to love when good labs go horribly wrong.
 
I came.across a headline and read some of the article, so I was curious. Scientists discover that gold is a 'reactive metal' by accidentally creating a new material in the lab https://www.earth.com/news/discovery-that-gold-is-reactive-metal-by-creating-gold-hydride-in-lab-experiment/ From SLAC - A SLAC team unexpectedly formed gold hydride in an experiment that could pave the way for studying materials under extreme conditions like those found inside certain planets and stars undergoing...

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