100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
Btec Applied Science Unit 14 Assignment D (Full Assignment) R210,26   Add to cart

Essay

Btec Applied Science Unit 14 Assignment D (Full Assignment)

1 review
 446 views  10 purchases
  • Course
  • Institution

This is Btec Applied Science Unit 14 Assignment D (Making designer chemicals) which was awarded a distinction and contains all the practical results. This is an example of a Distinction level assignment, and you may use it as a guide to help you achieve a distinction and finish this assignment.

Preview 2 out of 15  pages

  • August 31, 2023
  • 15
  • 2022/2023
  • Essay
  • Unknown
  • A+

1  review

review-writer-avatar

By: issatobe • 5 months ago

Really good assignment quality work and a good guide to use as as an assignment helper use if stuck with asseignment 14d

avatar-seller
Unit 14: Applications of Organic Chemistry
D: Investigate organic chemistry reactions in order to gain skills in preparative organic chemistry.
Assignment Title: Making designer chemicals


Ethyl Ethanoate: Ethyl acetate (also known as ethyl ethanoate, acetic acid ethyl ester, acetoxy ethane,
1-acetoxyethane, EtOAC, ETAC, EA) is an organic ester compound with the molecular formula C4H8O2.
It's a clear liquid with a fruity odour that's commonly found in glues and nail polish removers.
Preparation of ethyl ethanoate:
Mechanism: By combining ethanol with ethanolic acid and utilising concentrated sulfuric acid as a
catalyst, ester ethyl ethanoates are created. This process can be reversed and is gradual. To lessen the
likelihood of reverse reactions, esters are immediately removed using distillation.


For the purpose of making the ensuing
mechanics clear, all stages are displayed as one-way reactions. The formulation of the process is
impacted since the reverse reaction occurs in a totally different manner.
Concentrated sulfuric acid releases protons (hydrogen ions) to acetic acid in the first stage. A proton is
taken up by one of the single pairs of oxygen double-bonded to carbon, which then binds to carbon.




This illustration of the structure is inaccurate because oxygen acquires a positive charge when a proton
is transferred to it. The majority of the positive charge is spread among the carbon atoms, which are
located along the right edge of the ion. To put it another way, we may think of this structure as the
outcome of electron pair changes.

, As seen by the two arrows, each of the many configurations contributes to the ion's overall structure.
The connection will not automatically transition between her two separate setups as a result. Resonance
structures or canonical forms refer to several sorts of structures. The atoms of carbon and oxygen each
have a little positive charge. Each bond—which can range in size from single to double—between two
oxygen and carbon atoms is identical.
The positive charge on the carbon atom is attacked in step 2 by one of the lone pairs of electrons on the
oxygen atom of the ethanol molecule.




A proton (hydrogen ion) travels from the lower oxygen atom to the upper oxygen
atom in the third step. A other component of the mixture picks it up, and it is then approximately
reflected back to an oxygen atom. By forming a bond with an unpaired electron on the unreacted
ethanol molecule, this is accomplished. The finished item appears as follows:




Water molecules and ions are split apart in step 4. Production ions are now closely resembling the
finished product and are displayed in a fashion that represents it. The youngest ion has the same
structure as that described in step 1 in this process. Actually, the positive charge is dispersed along the
ion's edges, and the positioning of the charge on one of the oxygen
atoms also plays a role.




Step 5 involves removing hydrogen from oxygen by interacting with the bisulphate ions produced in step
1.




The ester was prepared and the sulfuric acid catalyst was renewed.

The benefits of buying summaries with Stuvia:

Guaranteed quality through customer reviews

Guaranteed quality through customer reviews

Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.

Quick and easy check-out

Quick and easy check-out

You can quickly pay through EFT, credit card or Stuvia-credit for the summaries. There is no membership needed.

Focus on what matters

Focus on what matters

Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!

Frequently asked questions

What do I get when I buy this document?

You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.

Satisfaction guarantee: how does it work?

Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.

Who am I buying this summary from?

Stuvia is a marketplace, so you are not buying this document from us, but from seller a-am. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy this summary for R210,26. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

85443 documents were sold in the last 30 days

Founded in 2010, the go-to place to buy summaries for 14 years now

Start selling
R210,26  10x  sold
  • (1)
  Buy now