- •Choose the correct range of acidity increase for the following compounds.
- •Formic acid
- •*Formic acid
- •Choose the correct range of acidity increase for the following compounds.
- •What is the identity of the intermediate (a) and the end-product (b) in the
- •To which group of lipids do terpenes belong?
- •Which group of compounds does borneol belong?
- •Which group of compounds does α-pinene belong?
- •Determine what compound will form after the glucose oxidation by Felling reagent:
- •What reaction do monosaccharides in the cyclic form?
ten
*
Glucose can react in the open and cyclic form. Glucose interacts with: 1)Br2 (H2O); 2) HNO3; 3) (CH3CO)2O; 4) [Ag(NH3)2]OH; 5)CH3OH (HCl). Which of the following reactions does glucose give in the cyclic form?
*3, 5
1, 3
3, 4
2, 5
1, 2
Which isomers of monosaccharides are called anomers? Choose the correct definition.
the cyclic forms of mannoses that differ only in their configuration at the С3
the cyclic forms of mannoses that differ only in their configuration at the С2 and С3
*the cyclic forms of mannoses that differ only by the position of hemiacetal hydroxyl
the cyclic forms of mannoses that differ only in their configuration at the С2
the cyclic forms of mannoses that differ only in their configuration at the С5
The change of the specific rotation of the freshly prepared monosaccharides solution is called:
inversion
isomerization
tautomery
epimeryzation
*mutarotation
Which of the following monosaccharides does belong to hexoses?
xylose
*mannose
arabinose
ribose
lyxose
Which of the following monosaccharides does belong to hexoses?
xylose
ribose
arabinose
*glucose
lyxose
Which of the following monosaccharides does belong to hexoses?
*galactose
xylose
arabinose
ribose
lyxose
Which of the following monosaccharides does belong to hexoses?
xylose
lyxose
arabinose
ribose
*fructose
Which of the following monosaccharides does belong to pentoses?
*xylose
mannose
glucose
fructose
galactose
Which of the following monosaccharides does belong to pentoses?
glucose
mannose
*arabinose
fructose
galactose
Which of the following monosaccharides does belong to pentoses?
glucose
mannose
galactose
*ribose
fructose
Which of the following monosaccharides does belong to pentoses?
fructose
mannose
galactose
glucose
*lyxose
Which of the following monosaccharides does belong to ketoses?
xylose
mannose
*fructose
ribose
arabinose
Which of the following monosaccharides does belong to ketohexoses?
xylose
mannose
*fructose
ribose
lyxose
Which of the following monosaccharides does belong to aldohexoses?
xylose
ribose
fructose
*mannose
arabinose
Which of the following monosaccharides does belong to aldohexoses?
xylose
*glucose
fructose
ribose
arabinose
Which of the following monosaccharides does belong to aldohexoses?
xylose
arabinose
fructose
ribose
*galactose
Which of the following monosaccharides does belong to aldopentoses?
*xylose
mannose
fructose
galactose
glucose
Which of the following monosaccharides does belong to aldopentoses?
fructose
mannose
*ribose
galactose
glucose
Which of the following monosaccharides does belong to aldopentoses?
galactose
mannose
fructose
*arabinose
glucose
Cyclic forms of monosaccharides in the chemical condition are:
cyclic ethers
*cyclic hemiacetals
cyclic esters
anhydrides
cyclic hemiketals
The mutarotation is cased by:
the change of the configuration at the last asymmetric carbon atom
epimeric transformations of the monosaccharides
*mutual transformations of the monosaccharides formf in the solution and achievement of the equilibrium between them
the change of the monosaccharides cyclic forms configuration
the change of the configuration at the С4
The hydroxyl-group, which is formed by monosaccharides cyclization is called:
*hemiacetal hydroxyl
epimeric hydroxyl
anomeric hydroxyl
hemiketal hydroxyl
enolic hydroxyl
The hydroxygroup, which is formed by monosaccharides cyclization is called:
epimeric hydroxyl
*glycosidic hydroxyl
anomeric hydroxyl
hemiketal hydroxyl
enolic hydroxyl
D-glucose and D-mannose are epimers, because:
have an equal number of chiral carbon atoms
have the different configuration of the fifth carbon atom
have the different number of the chirality centers
are the members of the same stereochemical range
*have the different configuration of the second carbon atom
Phenomenon, which is cased by the change of the sucrose solution specific optical rotation during the hydrolysis, is called:
epimerization
isomerization
*mutarotation
inversion
tautomery
Monosaccharides in the crystalline state have:
cyclic struscture
alicyclic structure
epimeric forms
endiol structure
*structure that includes all tautomeric forms
Determine compound, which will form after the oxidation of D–fructose by concentrated nitrate acid:
D–gluconic acid
D–glucaric acid
D–mannite
*D–arabinaric acid
D–galacturonic acid
Determine compound, which will form after the oxidation of D–glucose by concentrated nitrate acid:
D–gluconic acid
*D–glucaric acid
D–mannite
D–arabinaric acid
D–galacturonic acid
Determine compound, which will form after the oxidation of D–mannose by concentrated nitrate acid:
D–gluconic acid
*D–mannaric acid
D–mannite
D–arabinaric acid
D–galacturonic acid
Determine compound, which will form after the oxidation of D–galactose by concentrated nitrate acid:
D–gluconic acid
*D–glucaric acid
D–mannite
D–galactaric acid
D–galacturonic acid
Determine compound, which will form after the D–galactose oxidation by bromine water:
*D–galactonic acid
D–glucaric
D–mannite
D–galactaric acid
D–galacturonic
Determine compound, which will form after the D–glucose oxidation by bromine water:
D–mannite
D–glucaric acid
*D–gluconic acid
D–galactaric acid
D–galacturonic acid
Determine compound, which will form after the D–mannose oxidation by bromine water:
D–gluconic acid
D–glucaric acid
D–mannite
*D–mannonic acid
D–galacturonic acid
Determine compound, which will form after the oxidation of D–ribose by concentrated nitrate acid:
D–gluconic acid
D–glucaric acid
D–ribonic acid
*D–ribaric acid
D–galacturonic acid
Determine compound, which will form after the oxidation of D–ribose by bromine water:
D–gluconic acid
D–glucaric acid
*D–ribonic acid
D–ribaric acid
D–galacturonic acid
Which isomers of monosaccharides are called epimers?
hexoses that are different by the configuration of two asymmetric carbon atoms
*hexoses that are different by the configuration of one asymmetric carbon atoms
hexoses that are different by the configuration of three asymmetric carbon atoms
hexoses that are different by the configuration of all asymmetric carbon atoms
hexoses that are different by the configuration of four asymmetric carbon atoms
What reaction do monosaccharides in the cyclic form?
*alkylation
epimeryzation
reduction
ozazones formation
hydrazides formation
Determine what compound will form after the glucose oxidation by Felling reagent:
sorbite + CO2
glucuronic acid + Cu2O
gluconic acid + Cu
glucaric acid + CuO
*mixture of the oxidation products + Cu2O
D–glucose in the sodium hydroxide solution during few days forms the mixture of monosaccharides, which consists of:
D–glucose and D–fructose
D–glucose and D–mannose
*D–glucose, D–mannose and D–fructose
D–glucose, D–galactose and D–mannose
D–glucose, D–galactose and D–fructose
Choose the reagent that can oxidize aldoses:
hydrochloric acid
acetic acid
phenylhydrazine
*bromine water
sodium hydroxide alcoholic solution
Choose the reagent that can oxidize aldoses:
hydrochloric acid
*nitrate acid
phenyl hydrazine
acetic acid
sodium hydroxide alcoholic solution
Which of the following reactions, characteristic for aldehydes, do monosaccharides give?
formation of hydrosulfite derivatives
formation of ethers
formation of esters
*formation of phenyl hydrazones
interaction with fuchsine sulfite acid
What disaccharide will give reaction with Tollens reagent?
sucrose
maltose
amylose
amylopectin
*cellulose
Choose the end product of the cellulose hydrolysis, which will form after its heating with mineral acids:
D-galactopyranose
*D-glucopyranose
D-fructofuranose
D-maltose
E-lactose
What reagents can be used to distinguish maltose and sucrose?
*Tollens reagent
Reaction with α-naphthalene
Felling liquid
Fuchsine sulfite acid
Trommer test
What product will form after the adding of an excess of nitric mixture to cellulose?
cellulose mononitrate
cellulose dinitrate
cellulose sulfate
*cellulose trinitrate (pyroxylin)
cellulose disulfate
What product will form after the cellulose interaction with acetic anhydride at the presence of conc. H2SO4 (catalyst)?
cellulose acetate
cellulose diacetate
cellulose xanthogenate
*cellulose triacetate
cellulose sulfate
What monosaccharide is a product of starch hydrolysis?
*glucose
fructose
mannose
ribose
galactose
To the heteropolysaccharides the following compound belongs:
starch
cellulose
methyl-D-galactopyranoside
deoxyribose
*chondroitin sulfate
Nonreducing disaccharide is the following one:
cellobiose
maltose
*sucrose
lactose
xylose
Which of the following polysaccharides is used in the pharmacy in the production of “polyglucin’ and “rheopolyglucin”?
*dextrans
dextrins
cellulose
pectines
inulin
Sucrose, maltose and lactose are disaccharides. They found wide application in the food industry and medicine. With which of the proposed reagents can be identified among of these disaccharides reducing and nonreducing?
H2SO4
NaOH
K2CO3
*[Ag(NH3)2]OH
CH3COOH
Disaccharide form by hydrolysis of polysaccharides. What disaccharide will form after the hydrolysis of starch?
pyrogalose
lactose
cellobiose
sucrose
*maltose
Cellulose belongs to the polysaccharides. Choose monosaccharide, which will form after the cellulose hydrolysis:
β- D -fructopyranose
α- D -glucopyranose
*β- D -glucopyranose
α- D -fructofuranose
β- D -glucofuranose
Which of the following sugars does not form brick-red precipitate after the heating with Felling reagent?
*sucrose
glucose
lactose
cellulose
mannose
Fraction of starch is:
cellulose
maltose
fructose
*amylose
glycogen
Choose monosaccharides that are structural elements of sucrose:
only glucose
*glucose, fructose
glucose, galactose
only fructose
fructose, mannose
Which of the following disaccharides will not react with Felling reagent?
lactose and maltose
lactose
maltose
cellobiose
*sucrose
Disaccharides form by hydrolysis of polysaccharides. What disaccharide will form after the cellulose hydrolysis?
lactose
maltose
*cellobiose
sucrose
pyrogalose
From the following compounds choose reducing disaccharide:
inulin
*lactose
stachyose
sucrose
fructose
Choose chemical name of lactose:
*β–D–galactosido–1,4–?–D–glucopyranose
β–D–fructofuranose
α–D–glucopyranosido–1,2–?–D–fructofuranose
α–D–glucopyranosido–1,4–?– D–dlucopyranose
β–D–glucopyranosido–1,4–?– D–glucopyranose
Choose chemical name of maltose:
β–D–galactose–1,4–?–D–glucopyranose
β–D–galactosido–1,4–?–D–fructofuranose
α–D–– glucopyranosido-1,2–?–D–fructofuranose
*α–D– glucopyranosido –1,4–?–D–glucopyranose
β–D-glucopyranosido –1,4–?–D–glucopyranosido
Choose chemical name of sucrose:
β–D–galactosido–1,4–?–D–glucopyranose
2-β–D–fructofuranose
*α–D–glucopyranosido–1,2–?–D–fructofuranose
α–D––glucopyranosido-1,4–?– D–glucopyranose
β–D–glucopyranosido –1,4–?– D–glucopyranose
Choose chemical name of cellobiose:
β–D–galactosido–1,4–?–D–glucopyranose
β–D–fructofuranose;
α–D–glucopyranosido–?–D–fructofuranose
α–D–glucopyranosido–1,4–?– D–glucopyranose
*β–D– glucopyranosido–1,4–?– D–glucopyranose
At the disaccharides hydrolysis the following compounds form:
esters
carboxylic acids and water
polysaccharides
1 molecule of Carbon (IV) oxide and water
*2 molecules of monosaccharides
At the lactose hydrolysis the following compounds form:
α-glucose and β-fructose
*β-galactose and α-glucose
2 molecules of β-glucose
2 molecules of β-galactose
2 molecules of α-glucose
At the maltose hydrolysis the following compounds will form:
α-glucose and β-fructose
β-galactose and α-glucose
2 molecules of β-glucose
2 molecules of β-galactose
*2 molecules of α-glucose
At the cellulose hydrolysis the following compounds will form:
α-glucose and β-fructose
β-galactose and α-glucose
*2 molecules of β-glucose
2 molecules of β-galactose
2 molecules of α-glucose
At the sucrose hydrolysis the following compounds will form:
*α-glucose and β-fructose
β-galactose and α-glucose
2 molecules of β-glucose
2 molecules of β-galactose
2 molecules of α-glucose
In nature, disaccharides may exist both independently and as a part of many glycosides of plant and bacterial origin. Which of the pointed compounds are nonreducing disaccharides?
cellobiose
lactose
maltose
*sucrose
starch
Sucrose relates to the nonreducing disaccharides. Sucrose is decomposed into two monosaccharides after the hydrolysis. Indicate which monosaccharides are a part of sucrose molecule:
*glucose and fructose
glucose and glucose
glucose and galactose
mannose and fructose
fructose and fructose
It is known, that soaps are a salts of higher carboxylic acids (HCA). Which soap has a liquid consistency and is named as “green soap”?
calcium
sodium
*potassium
lithium
antimony
What reagent will characterize camphor as ketone?
HCl
Br2
NH3
CH3COOH
*C6H5NHNH2
What reagent can be used to confirm unsaturated character of camphor?
oxidation on the air
*bromine water
HNO3
HNO2
H2SO4
What reagent can be used to get “liquid soap” by the alkaline hydrolysis of fats (saponification)?
*K2CO3
NаOH
CаO
PbO
NaHCO3
Stearic acid belongs to the fats content. Chose formula of this acid:
C17H33COOH
*C17H35COOH
C15H31COOH
C17H31COOH
C19H33COOH
By the chemical structure fats belong to:
salts
*esters
carboxylic acids
alcohols
aldehydes
Alkaline hydrolysis of fats has name:
*saponification
hydration
hydratation
oxidation
hydrolysis
For the transformation of liquid fats into the solid fats the following reaction is used:
sulfonation
chlorination
bromination
*hydration
oxidation
Prostaglandins in their content have:
10 carbon atoms
30 carbon atoms
25 carbon atoms
*20 carbon atoms
15 carbon atoms
