
(a)
Interpretation:
The products obtained from the reaction of lactobionic acid and
Concept introduction:
The hydrolysis of the disaccharides is done in the presence of acid as a catalyst. The hydrolysis of the disaccharide is the breaking of the glycosidic linkage to give two monosaccharides units. Glycosidic linkage is an acetal linkage and acetal linkage hydrolysis takes place in the presence of an acidic solution.
(b)
Interpretation:
The products obtained from the reaction
Concept introduction:
The methylation of the hydroxyl group of sugars is an important reaction. The methylation of hydroxyl groups is done with the help of methylating agent, dimethyl sulfate in the presence of strong base sodium hydroxide.
(c)
Interpretation:
The products obtained from the reaction product of part (b) and
Concept introduction:
The hydrolysis of the disaccharides is done in the presence of acid as a catalyst. The hydrolysis of the disaccharide is the breaking of the glycosidic linkage to give two monosaccharides units. Glycosidic linkage is an acetal linkage and acetal linkage hydrolysis takes place in the presence of an acidic solution.

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Chapter 24 Solutions
Organic Chemistry Study Guide and Solutions
- Synthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forward
- Indicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate 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_forward
- Question 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_forwardIndicate 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_forward
- 2,2-Dimethylpropanal and acetaldehyde are reacted with sodium ethoxide in ethanol. Indicate the products obtained.arrow_forwardAdd 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_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
