Discuss the advantages/disadvantages of using chemically synthesized esters in place of natural esters in food. Support your opinion with references

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    Discuss the advantages/disadvantages of using chemically synthesized esters in place of natural esters in food. Support your opinion with references.

  31. Chemistry

    What are advantages/disadvantages to using esters in foods?

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  33. 12 Chemistry

    So I forgot, but I have one more I want to check while I am here (I seriously have a need for perfection, and want to include all of the details I can :P). So, what evidence is there that the esters synthesized in the lab are soluble? Again, thank you so

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    I have a really urgent question. I am wondering wheter or not esters are polar and what types of intermolular forces they have. can anybody answer this question nvm

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  53. Chem.

    On the topic of esters, if my Ester is CH3-C(double bond directly downward below the C)-O-CH3, would it be methyl ethanoate or methanoate ethyl? Thanks.

  54. Chem.

    As a go through my study guide, I'm finding that I'm getting esters and normal stoic acids confused. How can you tell when a stoic acid is an ester and when its not? Or are they always the same thing? Thanks for explaining this.

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    Why is the carbonyl group in tert-butoxycarbonyl group (tBOC) less susceptible to attack from nucleophiles than the carbonyl group in esters such as ethyl acetate? Is this something to do with conjugation?

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    Reaction 1 ............................O ...........................// CH2=CH-CH-OH + CH3-CH-CH2-C ........|...........|......\ .......CH3.........CH3......OH Left of the "+" is COMPOUND 1 and the right is COMPOUND 2. a) Identify the Functional groups in

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