Reactions of Monosaccharides

0.0(0)
studied byStudied by 0 people
GameKnowt Play
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
Card Sorting

1/26

flashcard set

Earn XP

Description and Tags

Vocabulary-style flashcards covering key concepts from the notes on monosaccharide reactions (oxidation, reduction, glycoside formation, phosphate esters, and amino sugars).

Study Analytics
Name
Mastery
Learn
Test
Matching
Spaced

No study sessions yet.

27 Terms

1
New cards

Aldose

A sugar that contains an aldehyde group at the terminal carbon.

2
New cards

Aldonic acid

Product formed when the aldehyde end of an aldose is oxidized by weak oxidizing agents.

3
New cards

Tollens solution

A weak oxidizing reagent that oxidizes the aldehyde end of an aldose to an aldonic acid and reduces Ag+ to Ag.

4
New cards

Benedict’s solution

A weak oxidizing reagent that oxidizes the aldehyde end of an aldose to an aldonic acid and reduces Cu2+ to Cu+, indicated by a red precipitate when glucose is present.

5
New cards

Reducing sugar

A sugar (typically an aldose) that can act as a reducing agent; ketoses can also act as reducing sugars under basic conditions after isomerization.

6
New cards

Lobry de Bruyn–Van Ekenstein transformation

Base-catalyzed isomerization that can convert ketoses to aldoses (and vice versa), enabling ketoses to act as reducing sugars.

7
New cards

Urine glucose test

Testing for the presence of glucose in urine, used as a diagnostic indicator for diabetes.

8
New cards

Aldaric acid

A dicarboxylic acid produced when a strong oxidizing agent oxidizes both ends of a monosaccharide.

9
New cards

Aldaric acids

Plural term for dicarboxylic acids formed from monosaccharides by strong oxidation.

10
New cards

Alduronic acid

Product of enzymatic oxidation at the primary alcohol end of an aldose, without oxidizing the aldehyde group.

11
New cards

Enzymatic oxidation

Oxidation of a monosaccharide in biological systems by enzymes, can yield alduronic acids.

12
New cards

D-Glucitol (sorbitol)

Sugar alcohol formed by reduction of glucose; used as a moisturizing agent and sweetener; linked to cataract formation when accumulated in the lens.

13
New cards

Alditol

Sugar alcohols obtained by reducing aldoses or ketoses.

14
New cards

Erythritol

An alditol commonly found in foods; a sugar alcohol.

15
New cards

D-Mannitol

An alditol used as a sweetener and in medical applications.

16
New cards

Xylitol

An alditol used as a sugar substitute in chewing gums and confections.

17
New cards

Glycoside

An acetal formed from a cyclic monosaccharide by replacing the hemiacetal OH with an OR group; exists in alpha and beta forms.

18
New cards

Glucoside

A glycoside derived from glucose.

19
New cards

Galactoside

A glycoside derived from galactose.

20
New cards

Phosphate ester formation

Reaction of monosaccharide hydroxyl groups with phosphoric acid to form phosphate esters, common in metabolism.

21
New cards

Phosphate ester

An ester formed between phosphate and a sugar hydroxyl; stable in water and important in carbohydrate metabolism.

22
New cards

Phosphate esters of glucose

Glucose molecules bearing phosphate esters; play key roles in carbohydrate metabolism.

23
New cards

Amino sugar

A monosaccharide in which one hydroxyl group (often at C-2) is replaced by an amino group; many have N-acetyl derivatives.

24
New cards

N-acetyl derivatives

Acetylated amino sugars commonly found in polysaccharides and as RBC markers.

25
New cards

Chitin

A polysaccharide built from amino sugars (e.g., N-acetylglucosamine), found in exoskeletons and fungal cell walls.

26
New cards

Hyaluronic acid

A glycosaminoglycan composed of amino sugars; an important component of connective tissue.

27
New cards

Red blood cell markers

Biochemical markers on red blood cells that include amino sugars and their derivatives.