
Interpretation:
From the structure of the alkoxide ion represented by the model, formed by the addition of a nucleophile to a
Concept introduction:
Esters are hydrolysed to carboxylic acids and alcohols both in the presence of acid and base catalysts. The base catalysed hydrolysis takes place in three steps i) The nucleophilic attack of the base on the ester carbonyl group ii) Elimination of the leaving group iii) Exchange of protons.
To identify:
From the structure of the alkoxide ion represented by the model, formed by the addition of a nucleophile to a carboxylic acid derivative, the nucleophile, the leaving group, the starting acid derivative and the ultimate product.

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Chapter 21 Solutions
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- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forward
- Indicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are mixed with sodium ethoxide in ethanol.arrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are reacted with sodium ethoxide in ethanol.arrow_forward2,2-Dimethylpropanal and acetaldehyde are reacted with sodium ethoxide in ethanol. Indicate the products obtained.arrow_forward
- Add conditions above and below the arrow that turn the reactant below into the product below in a single transformationADS fint anditions 百 Abl res condinese NC ง Add on condtions 1.0 B H,N.arrow_forward3. Provide all the steps and reagents for this synthesis. OHarrow_forwardSteps and explanationarrow_forward
- Steps and explanations please.arrow_forwardSteps on how to solve. Thank you!arrow_forward3. Name this ether correctly. H₁C H3C CH3 CH3 4. Show the best way to make the ether in #3 by a Williamson Ether Synthesis. Start from an alcohol or phenol. 5. Draw the structure of an example of a sulfide.arrow_forward
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