
Concept explainers
a.
To determine:
Whether the given carbohydrate (a.) is the alpha or beta anomer.
Introduction:
Diastereomers are those stereoisomers who differ in orientation of two chiral centers due to which the isomers are not the mirror images of each other. The cyclic forms of diastereoisomeric sugars which differ at the anomeric carbon (carbonyl carbon which reacts to form hemiacetal) are known as anomers. Hemiacetal is formed when the carbonyl carbon (partially positive) and oxygen of hydroxyl group (partially negative) forms a bond. The hemiacetal anomers exist in alpha and beta forms based on the site of substituent at anomeric carbon.
b.
To determine:
Whether the given carbohydrate (b.) is the alpha or beta anomer.
Introduction:
Diastereomers are those stereoisomers who differ in orientation of two chiral centers due to which the isomers are not the mirror images of each other. The cyclic forms of diastereoisomeric sugars which differ at the anomeric carbon (carbonyl carbon which reacts to form hemiacetal) are known as anomers. Hemiacetal is formed when the carbonyl carbon (partially positive) and oxygen of hydroxyl group (partially negative) forms a bond. The hemiacetal anomers exist in alpha and beta forms based on the site of substituent at anomeric carbon.

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Chapter 6 Solutions
General, Organic, and Biological Chemistry (3rd Edition)
- Predict the organic reactant that is involved in the reaction below, and draw the skeletal ("line") structures of the missing organic reactant. Please include all steps & drawings & explanations.arrow_forwardWhat are the missing reagents for the spots labeled 1 and 3? Please give a detailed explanation and include the drawings and show how the synthesis proceeds with the reagents.arrow_forwardWhat is the organic molecule X of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.arrow_forward
- What are is the organic molecule X and product Y of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.arrow_forwardAt 300 K, in the decomposition reaction of a reactant R into products, several measurements of the concentration of R over time have been made (see table). Without using graphs, calculate the order of the reaction. t/s [R]/(mol L-1) 0 0,5 171 0,16 720 0,05 1400 0,027arrow_forwardPredict the organic products that form in the reaction below, and draw the skeletal ("line") structures of the missing organic products. Please include all steps & drawings & explanations.arrow_forward
- What are the missing reagents for the spots labeled 1 and 3? Please give a detailed explanation and include the drawings and show how the synthesis proceeds with the reagents.arrow_forwardWhat are the products of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.arrow_forwardWhat would happen if you added the HCI to the Grignard reagent before adding benzophenone? Draw a reaction mechanism to support your answer.arrow_forward
- At 300 K, in the decomposition reaction of a reactant R into products, several measurements of the concentration of R over time have been made (see table). Calculate the order of the reaction. t/s [R]/ (mol L-1) 0 0,5 171 0,16 720 0,05 1400 0,027arrow_forwardWrite the correct IUPAC names of the molecules in the picturearrow_forwardHow many grams of solid NaCN have to be added to 1.5L of water to dissolve 0.18 mol of Fe(OH)3 in the form Fe(CN)63 - ? ( For simplicity, ignore the reaction of CN - ion with water) Ksp for Fe(OH)3 is 2.8E -39, and Kform for Fe(CN)63 - is 1.0E31arrow_forward
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