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WorksheetsQC (PQ) 100 - 200
Total questions: 99
Worksheet time: 50mins
Limit of moisture in non-aqueous titrimetric analysis is less than:
0.5%
0.05%
0.2%
0.02%
Standard solution in non-aqueous titrimetric analysis-acidimetry
Perchloric acid
Hydrogen bromide
Both A and B
None of the choices
Which of the following statement/s is/are correct?
I. Non-aqueous alkalimetry is used when the analyte is weakly acidic.
II. Non-aqueous alkalimetry is used when analyte is acid halide.
III. Non-aqueous alkalimetry is used when the analyte contains heterocyclic nitrogen compound.
IV. Non-aqueous alkalimetry is used when analyte is barbiturate.
I only
I and II only
I, II, and III only
I, II, and IV
Indicator/s used in non-aqueous titrimetry:
I. Nile blue III. Malachite green
II. Crystal violet IV. Phenolphthalein
I only
I and II only
I, II, and III only
I, II, III, and IV
Standard solutions in non-aqueous alkalimetry.
I. Lithium methoxide III. Hydrogen bromide
II. Perchloric acid IV. Sodium hydroxide
I only
I and II only
I, II, and III only
I, II, III, and IV
Perchloric acid in glacial acetic acid and perchloric acid in dioxane are volumetric solution used in what type of analysis?
Direct acidimetry
Direct alkalimetry
Non-aqueous acidimetry
Non-aqueous alkalimetry
A characteristic of a substance which is suitable for non-aqueous titrimetry is:
A.
Weakly reactive
B.
Weakly basic
C.
Very soluble in water
A and B
The strongest of the known common acids which gives excellent results in the assay of weak bases and its salts
Nitric acid
Sulfuric acid
Hydrochloric acid
Perchloric acid
A sample of Chlorpheniramine maleate weighing 0.502 g was assayed by non-aqueous titrimetry using 22.2 mL of perchloric acid with normality of 0.1125. Calculate the % purity of the sample. Each mL of 0.1 N perchloric acid is equivalent to 19.54 mg of C16H19ClN2.C4H4O4.
97.2
72.9
27.9
9.72
This method of precipitation titration with Silver involved the formation of a colored complex.
Mohr
Volhard
Fajan
A and B
Standard solution in precipitation method of analysis.
Disodium edentate
Silver nitrate
Sodium methoxide
Perchloric acid
Use to prevent one element from interfering in the analysis of another element.
Masking agent
Demasking agent
Both A and B
None of the choices
Argentometric titration is titration with _____ ion.
Magnesium
Sodium
Silver
Potassium
Fajans titration uses _____ indicator.
Acid base
Adsorption
Metal-ion
None of the choices
Ferric ammonium sulfate is used as indicator in the standardization of:
Silver nitrate
Ammonium thiocyanate
Edentate disodium
All of the choices
The end point in using ferric ammonium sulfate is:
White precipitate
Red-brown color
Pink color
Blue color
A molecule which provides groups of attachment to metal ions.
Ligand
Chelate
Both A and B
None of the choices
The following is/are true about EDTA titration.
I. EDTA titration is also known as complexometric titration.
II. The equilibrium constant in EDTA titration is called stability constant.
III. For end-point detection, commonly used indicator is called EDTA indicator.
IV. EDTA titration technique includes displacement titration.
I only
II and III
I, II, and III
I, II, and IV
Most of the official drugs containing Calcium and Magnesium are determined by:
Gravimetric
Complexometry
Bioassay
Non-aqueous matter
Adsorption indicators are used in:
Complexation reaction
Acidimetry
Volumetric precipitation
Alkalimetry
The indicator for EDTA titration against CaCO3 is:
Thymol blue
Hydroxynaphthol blue
Methyl red
Methylene blue
The primary standard used to standardize 0.05 M EDTA:
Calcium carbonate
Potassium biphthalate
Sodium oxalate
Calcium sulfate
The compleximetric method of determining metal ion is:
Volhard titration
EDTA titration
Permanganate titration
Kjeldahl
Adsorption indicators are used in
Neutralization
Precipitation
Complexation
Redox
The end point of a reaction in analysis by precipitation methods may be determined by using an instrument which is
Amperometric
Refractometer
Spectrometric
Chromatographic
A 0.2185 g sample of NaCl was assayed using Volhard method using 50 mL of 0.0998N silver nitrate and 11.9 mL of 0.1350 N ammonium thiocyanate. Calculate the % NaCl in the sample. MW NaCl = 58.45
42.6
62.4
90.5
6.24
A 50 mL aliquot of solution containing 450 g of Magnesium sulfate in 0.5 L required 37.6 mL of EDTA solution for titration. How many mg of Calcium carbonate will react with 1 mL of this EDTA solution? MW Magnesium sulfate = 120.37; MW CaCO3 = 100
0.9943 mg
9.99 mg
99.94 mg
994.3 mg
The type of chemical reaction involved for Fe2+ + Ce4- Fe3+ + Ce3- is a or an:
Acid base
Precipitation
Complex formation
Oxidation reduction
Other name of ferrous phenanthroline.
Eosin Y
Crystal violet
Ferroin
Ferric alum
Color of the complex resulting from reaction with ferrous phenanthroline
Blue
Red
Pink
Violet
Primary standard in the standardization of ceric sulfate solution
Potassium hydrogen phthalate
Calcium carbonate
Sodium bicarbonate
Arsenic trioxide/Sodium oxalate
A substance which gains electrons in a redox reaction.
Oxidizing agent
Reducing agent
Both A and B
None of the choices
Indicator in Redox Titration using KMnO4.
Starch TS
KMnO4
Methyl red TS
Methyl orange
Orthophenanthroline TS is used as indicator in:
Permanganometry
Ceric sulfate titration
Iodometry
Iodimetry
Which of the following statement/s is/are true?
I. KMnO4 can be standardized using arsenic trioxide.
II. KMnO4 serves as indicator in acidic solution.
III. Hydrogen peroxide can be analyzed using KMnO4.
IV. KMnO4 in acidic solution is reduced to colorless Mn+2.
I and II
I, II and III
II, III, and IV
I, III, and IV
Koppeschaar’s solution is also known as:
0.1 N Iodine solution
0.1 N Bromine solution
0.1 M sodium nitrite solution
0.1 N sodium thiosulfate solution
0.1N Bromine solution is employed as:
Oxidizing agent
Reducing agent
Masking agent
Demasking agent
Dichlorophenol-indophenol solution is standardized using:
Sulfanilamide USP
Ascorbic acid USP
Sulfathiazole USP
Resorcinol USP
The oxidation number of Mn in KMnO4 is:
+2
+1
+5
+7
Which of the following standard solutions is not used in redox titration?
Sodium thiosulfate solution
Iodine solution
Bromine solution
Sodium hydroxide solution
This method of analysis involve a change in valence of the reacting substances:
Neutralization
Precipitation
Complexation
Redox
Calculate the weight of oxalic acid required to prepare 1000 mL of 0.5 N of the solution. MW = 126
36.5 g
63.5 g
31.5 g
23.5 g
If starch TS is used as an indicator, the end point is/are:
Appearance of intense blue color
Disappearance of intense blue color
Both of the choices
None of the choices
Use of KI in the preparation of iodine solution.
Solubilizing agent
Change in pH of the solution
As preservative
All of the choices
Indicator in Iodometric method of analysis.
KMnO4
Methyl red TS
Methyl orange TS
Starch TS
The use of chloroform in sodium thiosulfate solution.
To stabilize the solution
To increase its solubility
To prevent bacterial growth
To maintain the pH of the solution
The use of sodium bicarbonate in the standardization of iodine solution
Increases the solubility
As buffer
As preservatives
To prevent bacterial growth
What is the use of HgI2 in the preparation of starch TS?
To increase the solubility of starch
To impart color
As a preservative
To stabilize the pH
The active fraction of starch which reacts with the iodine to form an intense blue color
Amylopectin
Amylose
Glucose
Sucrose
When a reducing analyte is titrated directly with iodine, the method used is called
Iodometry
Iodimetry
Cerimetry
Permanganometry
The 0.1N Iodine solution is standardized using:
Potassium permanganate
Potassium hydrogen phthalate
Arsenic trioxide
Sodium carbonate
Assay of sulfa drugs can be determined by this reaction with sodium nitrite.
Neutralization
Complexation
Precipitation
Diazotization
Which of the following volumetric solutions is used in diazotization analysis of sulfa drugs?
0.1 M sodium nitrite
0.05 Edentate disodium
0.01 M sodium nitrite
0.1 N Iodine solution
Phenol is assayed using this method of analysis.
Residual alkalimetry
Volumetric precipitation
Residual iodometry using excess bromine
Iodimetry
Assay of sodium nitrite is an example of what method of analysis
Direct titration – Redox
Indirect titration – Redox
Residual titration – Redox
Iodimetry
It is employed as an oxidizing agent in the assay of aniline, phenol and resorcinol
0.1 N Iodine
0.1 N Bromine
0.1 N Potassium
0.1 N Oxalic acid
The titrant in the assay of sodium hypochlorite solution is:
0.1 N Sodium thiosulfate
0.1N Iodine solution
0.1 N KMnO4
0.1 N Oxalic acid
The solubility of iodine in water is one gram of iodine is soluble in:
2920 mL
2930 mL
2940 mL
2950 mL
A 4.0570 g sample of chlorinated lime was mixed with enough water to make 1000 mL. A 100 mL of the mixture was treated with Potassium iodide and Acetic acid, then titrated with 22.4 mL of Sodium thiosulfate solution. A 20 mL sample of Sodium thiosulfate was found to be equivalent to 0.2996 g of pure iodine. Calculate the available chlorine in the sample. MW Iodine = 126.9; MW Cl = 35.45
27.35%
27.45%
29.02
23.1
A 0.5110 g samples of Sulfathiazole was assayed using 18.8 mL of 0.1005 M Sodium nitrite solution in a titration. Each mL of 0.1 M Sodium nitrite is equivalent to 25.53 mg of C9H9N3O2S2. Calculate the % C9H9N3O2S2 in the sample.
99%
95%
94%
93%
A sample of 0.1350 g of As2O3 was assayed iodimetrically using 23.4 mL of 0.1055 N iodine solution (Atomic Weights: As = 74.92, O = 16). The percentage purity of the sample is:
90.44
90.23
89.0
90.54
Twenty tablets of Ascorbic acid weighed 4.250 g and a powdered sample of 0.3075 g used up 21.5 mL of 0.1085 N iodine solution. What was the amount of Ascorbic acid per dose of 2 tablets? Each mL of 0.1 N iodine is equivalent to 8.80 mg of C6H8O6 (Ascorbic acid). The amount is:
283.7 mg
141.86 mg
0.2837 g
A and C
Which of the following statement/s is are correct according to USP 27?
I. In azeotropic method of water of analysis toluene is used as solvent.
II. In azeotropic method of analysis toluene and xylene are used as solvents.
III. In azeotropic method of analysis toluene, xylene, and water are used as solvents.
I only
I and II only
I, II, and III
None of the statement is correct
Which of the following statement/s is/are correct?
I. Method I of water content determination in USP 27 is the azeotropic toluene distillation method.
II. Method II of water content determination in USP 27 is the titrimetric method.
III. Method III of water content determination in USP 27 is the gravimetric method.
IV. Method IV of water content determination in USP 27 is the Karl Fischer method
I only
II only
III only
IV only
Primary standard used to standardize Karl Fischer reagent is:
Anhydrous sodium carbonated
Sodium tartrate
Potassium hydrogen phthalate
Sodium oxalate
Negligible is defined as a quantity not exceeding:
0.3 mg
0.4 mg
0.5 mg
0.6 mg
Ways to separate constituent in gravimetric analysis is/are
A.
Neutralization
B.
Physical means
C.
Chemical means
B and C
The laws and theories of chemistry involved in the chemical reaction in gravimetric analysis are:
Reversible reaction
Solubility product principle
Common-ion effect
All of the choices
If a 0.47 g sample of Potassium iodide yielded 0.7564 g of Silver iodide precipitate by gravimetric assay, compute for the % purity of the Potassium iodide. MW KI = 165.90; MW AgI = 234.76.
83.7%
93.7%
103.7%
113.7%
To determine the total ash, the sample is incinerated at a temperature of 675 ±25 0C. This temperature is represented by:
Very dull red heat
Dull red heat
White red heat
Bright red heat
Which of the following chemicals is not included in preparing the Karl Fischer reagent?
Pyridine
Acetone
Sulfur dioxide
Iodine
The type of ash where sulfuric acid is used to whiten the ash is:
Acid insoluble ash
Sulfated ash
Loss on ignition
ROI
Karl Fischer method of determining moisture is also called:
Toluene
Dew point
Titrimetric
Azeotropic
The temperature in 0C of ignition described as dull red heat is:
500 – 1000
550 – 700
500 – 750
300 – 450
The acid-insoluble residue derived from the soil adhering to the drug is:
Crude oil
Cellulose
Silica
Inorganic matter
A place to perform test with obnoxious, suffocating fumes is
Laminar flow hood
HEPA filter
Fume hood
A and B
It is use in the ignition of most drugs and precipitates:
Plain crucible
Evaporating dish
Goch crucible
Watch glass
Calculate the water content of Streptomycin powder using 3.50 g sample. The water equivalent factor, F, of the KF reagent was 4.6 and the volume consumed was 9.2 mL. The % water content is:
1.20
1.21
12.10
1.10
Calculate the water equivalence (F) of Karl Fischer reagent if a 250 mg sample of Sodium tartarate dehydrate required 18.5 mL of Karl Fischer reagent.
1.28 mg/mL
1.35 mg/mL
2.12 mg/mL
2.30 mg/mL
Each mL of the Karl Fischer reagent is equivalent to how much mg of water?
2
3
4
5
Karl Fischer electrometric titration method is specific only for the analysis of:
Food
Water
Gas
Air
Hexane is the best solvent in extracting:
Resins
Fats
Volatile oil
Acid
The crude fiber of a drug usually consists of:
Cellulose
Cholesterol
Phytosterol
All of the choices
The unsoponifiable matter present in vegetable oils and fats is:
Cholesterol
Cellulose
Phytosterol
Lard
A one percent (1%) solid in liquid solution is officially (USP) understood as:
1 g in 100 mL
100 mg in 1 mL
10 g in 100 mL
10 g in 1 L
The soluble constituent of a crude drug in a certain solvent is called:
Extractive
Ash
Crude fiber
Unsaponifiable matter
To separate immiscible solvent effectively, it is necessary to use:
Graduated pipet
Separatory funnel
Filter funnel
Xylene tube
Which of the following statement/s is/are correct?
I. Iodine value is a quantitative measure of the amount of unsaturated fatty acid in fats.
II. Method I of determining iodine value is also known as Hanus method.
III. Wij’s method is also a method determining iodine value.
IV. Hübl’s method is official method of determining iodine value.
I only
I and II
I, II, & III
All of the statements are correct
Koettsdorfer number is also known as
Acid value
Saponification value
Ester value
Iodine value
Method II of determining Iodine value is also known as:
Hübl method
Wij’s method
Hanus method
All of the choices
When the alcoholic KOH is used to neutralize the acid and saponify the ester of 1 gram of the oil or fat, the constant determined is:
Acid value
Ester value
Hydroxyl value
Saponification value
The iodine value of an oil is a quantitative measure of:
Phenol content
Saturated fatty acid
Unsaturated fatty acid
Unsaponifiable matter
The ester value determination of substances is applicable to the following, except
Fats
Volatile oils
Alcohols
Fatty oils
The number of mg of KOH required to saponify the esters in fat or oil is:
Saponification value
Ester value
Acid value
Iodine value
The ester value determination of substance is applicable to fats, oil and other, similar substances, whereas unsaponifiable matter is applicable fats and oil that are not saponified by:
Water
Alcohol
Alkali hydroxide
Acetone
If 10 g of olive oil required 20 mL of 0.0211 N NaOH in the titration of the free fatty acids. What is the acid number of the oil?
2.9
2.4
11.50
115
Determine the Iodine value of an unknown sample of oil weighing 0.21 g if 26 mL and 12 mL of 0.1100 N of Sodium thiosulfate are required for the blank and residual titration respectively.
90
93
108
200
If a sample of white wax is found to have an ester value of 65.7 and a saponification value of 74.2, what is the acid value of the sample?
8.5
86.5
186.5
56.5
The oil from peppermint spirit can be determined by using
Cassia flask
Babcock bottle
Pycnometer
Titration
