Histotechnology Quiz
docx
keyboard_arrow_up
School
Irvine Valley College *
*We aren’t endorsed by this school
Course
1A
Subject
Chemistry
Date
Jun 10, 2024
Type
docx
Pages
5
Uploaded by DoctorRedPandaPerson1151
Histotechnology Quiz
2.Acetic acid cause swelling of tissue. On the other hand, piric acid, mercuric acid, and ethanol all cause tissue to shrink, Bouin solution, a fixative compound, balance the effects by combining acetic acid with piric acid.
When processing delicate specimens using a standard closed tissue processor, dehydration should be done
by which of the following methods to minimized tissue distortion?
A graded series of reagents of increasing concentration
A graded series of reagents of decreasing concentration
A single reagent at a single concentration
Delicate specimens do not require a dehydration step
Dehydration should be done slowly. If the concentration gradient differs significantly between the inside and the outside of the tissue, the resulting diffusion currents could produce cell distortions. This is why slowly replacing the water through a graded series of increasing concetration is necessary to maintain proper structure before clearing and subsequent infiltration with a medium such as paraffin.
When orienting a tissue for embedding, which of the following tissues requires special attention to ensure it is cut in the cross section?
Brain
Liver
Fallopian Tubes
Muscle biopsies
Skin
While most tissues are embedded flat, some tissues require special orientation. Tubular structures, such as
fallopian tubes, should be embedded in cross section so that the lumen and all layers can be seen. Tissues with an epithelial surface, such as skin, are oriented so that they are cut in a place at right angle to the surface
Which of the following should be used for sectioning celloidin?
Rotary microtome
Sliding microtome
Clinical freezing microtome
Retracing microtome
Routine paraffin sections and frozen sections cut using a rotary microtome, which is the type found in most cryostats. Sliding microtomes are usesd for cutting celloidin and large paraffin blocks. The clinical freezing microtome, now replaced in most cases by cryostats, is used for preparing frozen sections. Finally, the retracting microtome is used for curring plastic sections.
Which of the following is a sign that the section was face too aggressively or quickly?
The tissue expands in the water bath
The section has numerous holes throughout
Some cells are in focus, whereas others are not
Chatter, or microscopic vibration, is seen in the section
Many problems can occur during microtomy. When sectioned too aggresively, tissues can have a moth-
eaten appearance, meaning they have many holes. Brain, live, and lymphnodes are especially prone to this
artifact. Other factors that can adversely affect the outcome of tissue sectioning include improper clearance angle of the knife and blade dullness/nicking.
Trichrome stains are primarily used to demonstrate which of the following?
Endogenous pigments
Components of the nervous system such as neurons and astrocytes
Differential demonstration of connective tissues such as muscle and collagen fibers
Bacterial infections
Trichrome stain is a term used to describe techniques that are able to differentiate muscle, collagen fibers,
fibrin, and erythrocytess. An example is the Masson Tricrhome stain in which muscle fibers are red, collagen is green, cytoplasm is light red, and nuclei are dark brown.
Mayer hematoxylin is chemically ripened with which of the following oxidants
Mercuric Oxide
Iodine
Potassium Iodate
Sodium Iodate
Hematoxylin itself is not a stain. It first must be oxidized to become hematin before it can be used as a stain. Hematoxylin can be oxidized naturally through exposure to light and air, but this process can take as long as 3-4 months. Hematoxylin can also be oxidized chemically using sodium iodate or mercuric oxide. Chemical oxidation occurs almost instantaneously.
Rhodamine and fluorescein isothiocyanate (FITC) are both exaamples of what?
antibodies
antigens
enzymes
fluorochromes
Fluorochromes are dyes that an be conjugated to antibodies, which can then be used to fluorescently label
specfic targets in tissues or cells by immunohistochemistry. This labelling can then be viewed by fluorescence microscopy or flow cytometry.
Which of the following can be used a "blurring" agent for alum hematoxylin when performing an H&E stain?
005% ammonia in distilled water
Glacial acetic acid
Glycerin
Copper
Alum hematoxylins stain nuclei red originally. They do not produce the familiar blue color until after the tissue section has been washed in a weak alkali solution. Hard tap water is usually alkaline enough to work, but other reagents that could be used include 0.05% ammonia in distilled water or saturated lithium carbonate.
The Von Kossa Stain is used to determine what?
The von Kassa stain is an indirect method for detecting calcium in a tissue. the silver reacts with anions of
the calcium salts such as phosphate and carbonate. Bright light is then used to reduce the silver salt to metallic silver.
Your preview ends here
Eager to read complete document? Join bartleby learn and gain access to the full version
- Access to all documents
- Unlimited textbook solutions
- 24/7 expert homework help
``
When using the PAS-diastase digestions method, which of the following tissue components is removed by the diastase digestion?
Lipids
Mucin
Fibrin
Glycogen
The periodic acid-Schiff method is used to stain polysaccharides, mucosubstance, and basement membranes. If a diagnosis requires the differentiation of mucin versus glyogen, the 2 slides are prepared by the same method, but one of them undergoes a diastase digestion before PAS staining. This digestion step removes glycogen from the tissue, thus allowing differentiation of the two tissue compnents upon comparison.
How would you prepare 100mL of a 5% solution when you have a 20% solution available?
50mL of the 20% solution + 50mL if distilled water
60mL of the 20% solution + 40mL if distilled water
51mL of the 20% solution + 90mL if distilled water
25mL of the 20% solution + 75mL if distilled water
Which of the following can be an explosion hazard?
Oxalic acid
Liquid Nitrogen
Iodine
Piric Acid
Piric acid can be explosive when dry or when compled with metal; therefore, it must be kept wetted with a minimum of 30% water and must not be stored in metal containers or poured down the sink. Other chemicals that could potentially pose an explosion hazard include benzoyl peroxide and ammoniacal silver solutions.
Which of the following dye combinations is used in the classical Papanicolaou stain (Pap stain)?
Methylene blue and eosin
Malachite green and safranin
Weigert hematoxylin, acid fuchsin, and Light Green SF yellowish
Alum-hematoxylin, Orange G, Eosin Y, Light Green SF, and Bismark Brown Y
The dyes in the classical Pap stain, are used to stain the following tissue components;
hematoxylin stains nluclei
orange G stains keratin
eosin Y stains superficial squamous cells, nucleoli, erythrocytes, and cilia
light green SF stains intermediate squamous cells, parabasal and columnar cells, histiocytes,leukocytes, large- and small-cell carcinomas and cells from adenocarcinomas
Bismark brown Y tends to precipitate out of solution resulting in very little to no staining, and is often eliminated from contemporary formulations.
Related Documents
Related Questions
An organic chemistry laboratory Extraction; the extraction of crude naphtalene- benzoic acid mixture. Naphthalene is a suspect carcinogen and is toxic to aquatic life. Find an alternative pair of molecules that adhere better to the principles of green chemistry and can be separated by extraction using green' solvents. (kindly answer fully)
arrow_forward
A student use the same protocol as in the lab manual to extract benzoic acid, phenol, and naphthalene. Below are the steps he took
Step 1 - Dissolve all three in 15 ml ether and place in separatory funnel
Step 2- Add 15 ml of sodium carbonate and mix well
Step3 - Isolate the aqueous layer and Add hydrochloric acid, which resulted in a precipitate
Step 4- Add 15 ml of sodium hydroxide to the ether layer and mix
Step 5- Isolate the aqueous layer and add hydrochloric acid, which resulted in a precipitate.
Step 6- dry the ether layer and collect the solid that is left
arrow_forward
Refer to the following information to answer questions 1 to 9:
As a biotechnologist working for a pharmaceutical company, you as tasked with preparing the cardiac antiarrhythmic
agent Amelfolide from p-nitrobenzyl chloride and 2,6-dimethyl aniline (Figure 2.1). You are provided the starting
materials and asked to prepare 7.50g of pure material. No other instructions are given to you.
MW 2,6-dimethylaniline = 121.18 g/mol
MW p-nitrobenzyl chloride = 185.56 g/mol
MW Amelfoliode = 270.29 g/mol
%3D
NH2
CI
O2N
O2N
When developing a synthetic scheme, the first thing to do is check the scientific literature to see if someone has done
this reaction before you. Upon performing a literature search, you identify a publication where a group from Japan has
performed the same reaction you are tasked with completing. The paper is in Japanese and you cannot read the
details of the procedure, however, you can make out that the reaction is performed using DCM as the solvent and
proceeds with a yield of…
arrow_forward
Part B: Miscibility of liquids
1.
Place 10 drops of propan-2-ol into each of two DRY semi-micro test tubes.
2.
Add 10 drops of water to one test tube and 10 drops of cyclohexane to the other test tube, shake and observe whether
the two liquids in each test tube are miscible. Record your results then discard the contents of the test tubes into the
organic waste container.
3.
Place 10 drops of water in a clean semi–micro test tube and add 10 drops of cyclohexane to it. Record whether the two
liquids are miscible. If two layers form (i.e. the liquids are immiscible) add a drop of blue food dye to the mixture and
shake, then allow the two layers to reform. Based on your observation, decide whether the food dye is more soluble in
water or cyclohexane and then discard the mixture into the non–halogenated waste container.
Record whether the combinations of liquids shown below are miscible.
Water
Cyclohexane
Propan-2-ol
Cyclohexane
arrow_forward
A student use the same protocol as in the lab manual to extract 4 chloroanilline, benzoic acid and naphthalene. Below are the steps he took
Step 1 - Dissolve all three in 15 ml ether and place in separatory funnel
Step 2- Add 15 ml of hydrochloric acid and mix well
Step 3 - Isolate the aqueous layer and add sodium hydroxide which resulted in a precipitate
Step 4- Add 15 ml of sodium carbonate to the ether layer and mix
Step 5- Isolate the aqueous layer and add hydrochloric acid, which resulted in a precipitate.
Step 6- dry the ether layer and collect the solid that is left
arrow_forward
methyl alcohol and ethyl alcohol are poor extraction solvent. why?
arrow_forward
Melting Point Analysis Experiment
Objective:
The goal of this experiment is to determine the identity of an unknown organic compound based
on melting point analysis. The melting point range of the unknown compound will be
determined using a Mel-Temp apparatus. The identity of the compound will be determined by
comparing the measured melting point range to the literature melting point ranges of five
different compounds: imidazole, 4-nitrobenzaldehyde, mandelic acid, trans-cinnamic acid, and
D-(+)-gluconic acid 8-lactone.
Table of Constants: (To be completed before your lab period)
Compounds
Structure
Imidazole
4-nitrobenzaldehyde
mandelic acid
trans-cinnamic acid
D-(+)-gluconic acid
8-lactone
(Draw the skeletal structure of each
compound, including lone pairs)
HN
-N
Melting
Point (°C)
88 - 91
103-106
119-121
132 - 135
1154 - 162
Approximate
Mel-Temp
Setting (2
significant figures)
2.8
arrow_forward
Use the dropdown menus to indicate whether a solvent pair could be used successfully in a mixed-solvent recrystallization.
a-hexanes and water [ Select successful or unsuccessful ]
b-chloroform and diethyl ether [ Select successful or unsuccessful ]
c-acetone and methanol [ Select successful or unsuccessful ]
arrow_forward
Prelab Questions:
1. Write the balanced equation for the bromination of 4-methylbenzoic acid.
2. Complete the following table for the bromination with the values from the procedure given:
density,
g/mL
XXX
XXX
MW,
mp/bp, °C
mp, 179-181
mp, 175-180 (dec)
mp, 105
bp, 132
equiv mmol
compound
4-methylbenzoic acid
NBS
Benzoyl peroxide
chlorobenzene
g/mol
mL
XXX
XXX
XXX
XXX
XXX
XXX
XXX
XXX
3. What is the theoretical yield for this reaction?
arrow_forward
4
arrow_forward
Some organic solvents do not work well in liquid-liquid aqueous extractions. Ethanol (HOCH2CH3) is a common inexpensive solvent, but is a poor solvent for extractions. In ten or fewer words, provide an explanation for why ethanol is a poor solvent selection for extraction. Hint: you may want to look up various properties of the molecule.
arrow_forward
Give the flow diagram for the separation of 2-methoxvnaphthalene and trans-cinnamic acid by filling in the empty boxes with the correct
structures and reagents
OH
Add EtOAc
Add HaO
in H20
in EtOAc
Add EtOAc
Dry over MgSO, (anh)
Filter
Add
Distill off E1OAC
Dry over MgS0, (anh)
Filter
Distill off E10AC
Pure Compound
Pure Compound
Discard H,0 layer
arrow_forward
You are given a pure unknown compound with a melting point of 118 – 120°C, which is either mandelic acid (lit. mp = 118 -120°C) or succinic anhydride (lit. mp = 119 – 120°C), along with pure samples of mandelic acid and succinic anhydride. You determine the mp of an approximately 50:50 mixture of the unknown sample and succinic anhydride to be 118-120° C. What is the identity of the unknown sample?
a. succinic anhydride
b. mandelic acid
arrow_forward
please solve question 1 and 2, thanks alot sir for ur help, note that this is not a graded question, its a past paper
arrow_forward
2. A MgCl2 stock solution that is 25 mM is provided by a PCR kit. We will prepare a 10 ul
PCR reaction that needs to have a final concentration of 5 mM. How much of the stock
magnesium chloride do we need to add to our PCR reaction?
arrow_forward
Please tell me how to get this answer (step-by-step) including equations used. Thank you!
40 mL of a 35% v/v acetic acid solution is needed. In the stock room is a bottle of 50% v/v aceticacid. How much water should be used as the diluent?ANS: 12 mL of water is needed
arrow_forward
Answer the following questions following a Solubility and recrystalization lab for organic chemisty.
1. In a solubility and recrystallization lab you are working with the following chemicals : solids (benzoic acid, acetanilide,naphthalene, and resorcinol) and three solvents (water, ethanol and petroleumether) discuss and rank the polarity of the solvents and the polarity of the compounds being investigated.
2. Briefly describe how a mixture of sand and benzoic acid (soluble in hotwater) could be separated to produce pure benzoic acid.
arrow_forward
1.Toxicity Characteristic Leaching Procedure (TCLP)
2.Effect within minutes or days after exposure
3.Colorless gas used for the production of methanol
4. Mesothelioma
5. Combustion product that is associated with burning tire smell
6. Oral lethal dose in grams of a chemical with an LD50 of 1500 mg/kg for a 105 kg person
7. Effect several years after exposure
8. Product causes long-term chronic effects
9. Toxic pollutant that is associated with atmospheric haze
10. Federal drinking water standard for lead
Match with the following answer .
a)157.5 g,
b) Carbon monoxide
c) Sulfur dioxide
d) CPSC Toxicity Criteria
e) Chrysotile
f) RCRA Toxicity
g) 15 µg/L
h) Acute health effect
i) 71.6 g
j) Latent health effect
k) Nitrogen oxide
arrow_forward
Use a flow chart to show how you could separate a mixture of the following compounds using an
extraction. Be sure to include all steps to get pure materials.
arrow_forward
what is the chemical reaction for this procedure?
arrow_forward
SEE MORE QUESTIONS
Recommended textbooks for you

Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education

Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning

Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education

Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning

Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY
Related Questions
- An organic chemistry laboratory Extraction; the extraction of crude naphtalene- benzoic acid mixture. Naphthalene is a suspect carcinogen and is toxic to aquatic life. Find an alternative pair of molecules that adhere better to the principles of green chemistry and can be separated by extraction using green' solvents. (kindly answer fully)arrow_forwardA student use the same protocol as in the lab manual to extract benzoic acid, phenol, and naphthalene. Below are the steps he took Step 1 - Dissolve all three in 15 ml ether and place in separatory funnel Step 2- Add 15 ml of sodium carbonate and mix well Step3 - Isolate the aqueous layer and Add hydrochloric acid, which resulted in a precipitate Step 4- Add 15 ml of sodium hydroxide to the ether layer and mix Step 5- Isolate the aqueous layer and add hydrochloric acid, which resulted in a precipitate. Step 6- dry the ether layer and collect the solid that is leftarrow_forwardRefer to the following information to answer questions 1 to 9: As a biotechnologist working for a pharmaceutical company, you as tasked with preparing the cardiac antiarrhythmic agent Amelfolide from p-nitrobenzyl chloride and 2,6-dimethyl aniline (Figure 2.1). You are provided the starting materials and asked to prepare 7.50g of pure material. No other instructions are given to you. MW 2,6-dimethylaniline = 121.18 g/mol MW p-nitrobenzyl chloride = 185.56 g/mol MW Amelfoliode = 270.29 g/mol %3D NH2 CI O2N O2N When developing a synthetic scheme, the first thing to do is check the scientific literature to see if someone has done this reaction before you. Upon performing a literature search, you identify a publication where a group from Japan has performed the same reaction you are tasked with completing. The paper is in Japanese and you cannot read the details of the procedure, however, you can make out that the reaction is performed using DCM as the solvent and proceeds with a yield of…arrow_forward
- Part B: Miscibility of liquids 1. Place 10 drops of propan-2-ol into each of two DRY semi-micro test tubes. 2. Add 10 drops of water to one test tube and 10 drops of cyclohexane to the other test tube, shake and observe whether the two liquids in each test tube are miscible. Record your results then discard the contents of the test tubes into the organic waste container. 3. Place 10 drops of water in a clean semi–micro test tube and add 10 drops of cyclohexane to it. Record whether the two liquids are miscible. If two layers form (i.e. the liquids are immiscible) add a drop of blue food dye to the mixture and shake, then allow the two layers to reform. Based on your observation, decide whether the food dye is more soluble in water or cyclohexane and then discard the mixture into the non–halogenated waste container. Record whether the combinations of liquids shown below are miscible. Water Cyclohexane Propan-2-ol Cyclohexanearrow_forwardA student use the same protocol as in the lab manual to extract 4 chloroanilline, benzoic acid and naphthalene. Below are the steps he took Step 1 - Dissolve all three in 15 ml ether and place in separatory funnel Step 2- Add 15 ml of hydrochloric acid and mix well Step 3 - Isolate the aqueous layer and add sodium hydroxide which resulted in a precipitate Step 4- Add 15 ml of sodium carbonate to the ether layer and mix Step 5- Isolate the aqueous layer and add hydrochloric acid, which resulted in a precipitate. Step 6- dry the ether layer and collect the solid that is leftarrow_forwardmethyl alcohol and ethyl alcohol are poor extraction solvent. why?arrow_forward
- Melting Point Analysis Experiment Objective: The goal of this experiment is to determine the identity of an unknown organic compound based on melting point analysis. The melting point range of the unknown compound will be determined using a Mel-Temp apparatus. The identity of the compound will be determined by comparing the measured melting point range to the literature melting point ranges of five different compounds: imidazole, 4-nitrobenzaldehyde, mandelic acid, trans-cinnamic acid, and D-(+)-gluconic acid 8-lactone. Table of Constants: (To be completed before your lab period) Compounds Structure Imidazole 4-nitrobenzaldehyde mandelic acid trans-cinnamic acid D-(+)-gluconic acid 8-lactone (Draw the skeletal structure of each compound, including lone pairs) HN -N Melting Point (°C) 88 - 91 103-106 119-121 132 - 135 1154 - 162 Approximate Mel-Temp Setting (2 significant figures) 2.8arrow_forwardUse the dropdown menus to indicate whether a solvent pair could be used successfully in a mixed-solvent recrystallization. a-hexanes and water [ Select successful or unsuccessful ] b-chloroform and diethyl ether [ Select successful or unsuccessful ] c-acetone and methanol [ Select successful or unsuccessful ]arrow_forwardPrelab Questions: 1. Write the balanced equation for the bromination of 4-methylbenzoic acid. 2. Complete the following table for the bromination with the values from the procedure given: density, g/mL XXX XXX MW, mp/bp, °C mp, 179-181 mp, 175-180 (dec) mp, 105 bp, 132 equiv mmol compound 4-methylbenzoic acid NBS Benzoyl peroxide chlorobenzene g/mol mL XXX XXX XXX XXX XXX XXX XXX XXX 3. What is the theoretical yield for this reaction?arrow_forward
- 4arrow_forwardSome organic solvents do not work well in liquid-liquid aqueous extractions. Ethanol (HOCH2CH3) is a common inexpensive solvent, but is a poor solvent for extractions. In ten or fewer words, provide an explanation for why ethanol is a poor solvent selection for extraction. Hint: you may want to look up various properties of the molecule.arrow_forwardGive the flow diagram for the separation of 2-methoxvnaphthalene and trans-cinnamic acid by filling in the empty boxes with the correct structures and reagents OH Add EtOAc Add HaO in H20 in EtOAc Add EtOAc Dry over MgSO, (anh) Filter Add Distill off E1OAC Dry over MgS0, (anh) Filter Distill off E10AC Pure Compound Pure Compound Discard H,0 layerarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY

Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education

Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning

Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education

Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning

Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY