test 2 white -key(1)(1)
pdf
keyboard_arrow_up
School
University of Alabama *
*We aren’t endorsed by this school
Course
105
Subject
Chemistry
Date
Feb 20, 2024
Type
Pages
9
Uploaded by DeanWombat3042
1 CH105-002 Exam #2 Name____________________________ CWID_____________________________ MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question. 1. What functional groups are in the open-chain forms of monosaccharides? A.
Hydroxyl groups B.
Aldehyde groups C.
Ketone groups D.
Hydroxyl and aldehyde or ketone groups E.
Hydroxyl and ether groups 2. What is the classification of the following monosaccharide? A.
aldotriose B.
ketotriose C.
aldotetrose D.
ketotetrose E.
ketopentose 3. Disaccharides have two monosaccharide units joined together by a glycosidic bond. What is the monosaccharide units for the following disaccharide? A. ß-D-galactose and α
-D-glucose B. α
-D-galactose and α
-D-glucose C. ß -D-galactose and α
-lactose D. maltose and lactose
2 4. Which pairs of Fisher projections represent enantiomers? 5. Which of the following is the Fischer projection of the following molecule? 6. What is the classification of the compound shown below? A. L B. D C. A sugar this small is not classified as L or D.
A. B. C. D. A. B. C. D.
3 7. The sugar also is known as dextrose and blood sugar is A. sucrose. B. galactose. C. fructose. D. lactose. E. glucose. 8. What product forms when the compound below is treated with H
2
in the presence of a Pd catalyst? 9. Sucrose is a disaccharide. What is the glycosidic link in sucrose? A. α(1
6)-glycosidic bond B. α, β
(1
2)-glycosidic bond C. α(1
4)-glycosidic bond D. β
(1
4)-glycosidic bond 10. How many chiral centers in the following compound? A. B. C. D.
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
4 A. 1 B. 2 C. 3 D. 4 11. What is the Haworth structure for β
--L-glucose? 12. What hydrolysis products are formed when the following wax is treated with aqueous sulfuric acid? 13. What type of lipid is the following compound? A. B. C. D
. A. CH
3
(CH
2
)
18
CHO + CH
3
(CH
2
)
18
CH
2
OH B
. CH
3
(CH
2
)
18
COOH + CH
3
(CH
2
)
20
CH
2
OH C. CH
3
(CH
2
)
20
COOH + CH
3
(CH
2
)
16
CH
3
D. CH
3
(CH
2
)
20
COOH + CH
3
(CH
2
)
18
COOH E. CH
3
(CH
2
)
18
CH
2
OH + CH
3
(CH
2
)
16
COOH
5 A. sphingomyelin B. glycerophospholipid C. triacylglycerol D. wax 14. Compared to unsaturated fatty acids, saturated fatty acids have A. shorter carbon chains. B. lower melting points. C. weaker intermolecular attraction. D. higher melting points. E. longer carbon chains. 15. Choose the saturated fatty acid from the compounds below. A. B. C. D. 16. What is the condensed structural formula for the wax formed by the reaction of palmitic acid and cetyl alcohol? 17. Palmitic acid is a 16 carbon acid. In a balanced equation, the products of the saponification of glyceryl tripalmitate (tripalmitin) are A. B. C. D.
6 18. Which is a nonhydrolyzable lipid? 19. What is the main component of the cell membrane? A. triacylglycerols B. phospholipids C. steroids D. waxes 20. The transport of particles across a cell membrane from high concentration to low concentration is called 21. Fats and oils are structurally both triacylglycerols, but fats are solids at room temperature and oils are liquids at room temperature. Which statement best describes the reason for their difference in the physical state? A. B. C. D. A. a phospholipid B. a wax C. a triacylglycerol D. a cholesterol A. facilitated transport. B. diffusion. C. active transport. A. Fats are simple triacylglycerols and oils are mixed triacylglycerols. B. Oils are simple triacylglycerols and fats are mixed triacylglycerols. C. Oils contain longer fatty acid chains than fats do, and therefore have higher melting points than fats. D
. Fats contain a higher percentage of saturated fatty acids than oils do, and therefore have higher melting points than oils.
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
7 22. Which structure is the steroid skeleton? 23. Which compound has the highest boiling point? 24. Carboxylic acids are water-soluble due to their 25. What is the IUPAC name for the following ester? 26. What is the IUPAC name of the compound below? A. B. C. D. A. (CH
3
)
2
CHCH
2
CHO B. (CH
3
)
2
CHCH
2
CH
2
CH
2
OH C. CH
3
(CH
2
)
6
CH
3
D. CH
3
CH
2
CH
2
CH
2
CH
2
COOH A. nonpolar nature B. ionic bonds C. ability to hydrogen bond D. high melting points A. propyl propanoate B. propyl ethanate C. ethyl propanoate D. propyl ethanoate A. 2-methyl-2-butyl-1-propanoic acid B. 2,2-dimethylhexanoic acid C. 2-methyl-2-propylpropanoic acid D. 2,2-dimethyl-1-hexoic acid E. 5,5-dimethylhexanoic acid
8 27. What are the products of the acid
–
base reaction below? 28. What products are formed in the base hydrolysis of the ester shown below with NaOH? 29. What ester is formed when hexanoic acid is treated with methanol (CH
3
OH) in the presence of H
2
SO
4
? 30. What is the hydrolysis reaction of an ester by a base called? 31. Which statement concerning carboxylic acids is incorrect? A. The functional group of a carboxylic acid is abbreviated as COOH or CO
2
H. B. Carboxylic acids are hydrogen ion donors. A. B. C. D. A. B. C. D. A. B. CH
3
CH
2
CH
2
CH
2
COOCH
3
C. D. A. an addition reaction B. an esterification C. a substitution reaction D. a saponification
9 C. The presence of a carboxylic acid increases the [H
3
O
+
] in an aqueous solution relative to water. D. The reaction of a carboxylic acid with a strong base produces a water-insoluble carboxylate salt. 32. lactose, milk sugar, is a disaccharide found in milk and milk products. What kinds of monosaccharides are present in lactose? A. glucose + glucose B
. glucose + galactose C. glucose + fructose D. galactose + galactose 33. Chirality occurs when stereoisomers have mirror images that are
A. superimposable. B. the same. C. not superimposable. D. not visible to one another. E. identical.
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
Related Documents
Related Questions
Pls help ASAP. Pls circle the final answer
arrow_forward
3-Bromo-1-methylbenzene contains __________ halogens.
0
1
3
2
arrow_forward
Do not give handwriting solution.
arrow_forward
SC
Organic Functional Groups
Naming and drawing aldehydes
Draw the skeletal ("line") structure of 4,5-dihydroxypentanal.
Explanation
Click and drag to start drawing a
structure.
Check
80
F3
DOD
BOD F4
X
MacBook Air
: □
0*
1/5
Julianna
?
000
Ar
2024 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility
F12
F8
FIO
arrow_forward
PLEASE ANSWER QUESTION IN 15 MINTUES NOT MORE PLEASE AND THANK YOU. If you do answer the question correctly and post it in the next 15 minutes, NO NEED TO SHOW THE WORK, I JUST WOULD LIKE THE CORRECT ANSWER AS SOON AS POSSIBLE.
isnt the answer e)none of theses
since the correct : Structural Isomers
Optical isomers are the compounds which has the same number of atoms and bonds, but different type of spatial arrangement of bonds. The compounds as these isomers are non-superimposable mirror images of each other.
Structural isomers are the constitutional isomers in which two compounds has same molecular formula but different structures.
Stereoisomer are the compounds which have same number of atoms and bonds but differs by their spatial arrangement of atoms . Optical isomers are a type of stereo isomers.
Geometric isomers are the isomers which has same number of atoms and even same structural formula but these compounds differ in the arrangement of bonds. For example :…
arrow_forward
Please correct answer and don't use hand rating
arrow_forward
Can you please explain what this asking for ?
arrow_forward
Subject : chem
arrow_forward
Förčé Completion This test can be saved and resumed at any pc
Remaining Time: 58 minutes, 20 seconds.
Question Completion Status:
A Moving to another question will save this response.
Question 5
Draw at least 5 isomers for C5H11C1?
Attach File
Browse My Computer
A Moving to another question will save this response.
arrow_forward
List answer using letters not structures. Thank you!
arrow_forward
Question 20
A carbohydrate can be defined as a molecule
O whose name ends in "-ase".
composed of carbon atoms bonded to water molecules.
O composed of amine groups and carboxylic acid groups bonded to a carbon skeleton.
that is an aldehyde or ketone and that has more than one hydroxyl group.
O composed mostly of hydrocarbons and soluble in non-polar solvents.
Question 21
arrow_forward
19. Draw the structure for the compound at the bottom of the page. Show your reasoning.
C3H1403
100
80
4880
3580
3000
2568
2000
1500
1000
2H
3H
3H
2H
2H
2H
4.5
4.0
3.5
3.0
2.5
2.0
1.5
1.0 PPM
9LC42 86 9
1745.80
BL
SS LIC
1486.89
1387. 12
852.85
O 208
arrow_forward
In an addition reaction, the starting material contains a(n) _____________.
halogen
alcohol
ring
pi bond
carbocation
arrow_forward
tempt.php?attempt%3D33606
You are logged in as 319
-ORGANIC CHEMISTRY FOR MEDICAL STUDENTS-1-7
Question 1
Number of stereogenic centers in 1,3-dibromo-1-chloropentane is:
Not yet answered
Marked out of 3.00
V Flag question
Select one:
a. 1
b. 3
O c. 0
d. 2
G 4) O ENC
F6
F7
F8
PrtSc
Insert
Delete
F9
F10
F11
F12
arrow_forward
doublet 2H
triplet 2H
triplet 1H
P-M
NO.
B.
selectone.
Ne
Previous pag
arrow_forward
1a. draw condensed structure for 2,3 dimethylbutane.
1b. next draw condensed structures for a linear isomer and a branched isomer of that compound and name the compounds.
1c. Mn2+ + BiO3 >(Arrow) MnO4 - + Bi3+
Oxidized:
Oxidizing agent:
Reduced:
Reducing Agent:
arrow_forward
question 1 and 2
arrow_forward
please answer 2 and 3
arrow_forward
The following chemical equation is for an addition reaction, where the important atoms, groups, and bonds
involved have been highlighted for you:
4
+
+CI-CI
Use the information provided to predict the missing organic product and draw its structure in the drawing
area below. Make sure to use the same skeletal ("line") style for the structure as the rest of the equation.
Explanation
?
Click and drag to start drawing a
structure.
Check
Ⓒ2023 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center Accessibility
577
Se
MAY
arrow_forward
Complete the mechanism for the generation of the electrophile used for Friedel-Crafts acylation with the given acyl halide.
Add curved arrows, bonds, electron pairs, and charges where indicated.
Step 1: add a curved arrow.
Step 2: complete the structure and add a
|curved arrow.
Select
Draw
Rings
More
Erase
Select
Draw
Rings
More
Erase
a Fe
H
: a :
ci :
|
Fe
Fe
CI
: a :
: c :
Q 2 Q
↑
:
|
arrow_forward
SEE MORE QUESTIONS
Recommended textbooks for you

Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Related Questions
- SC Organic Functional Groups Naming and drawing aldehydes Draw the skeletal ("line") structure of 4,5-dihydroxypentanal. Explanation Click and drag to start drawing a structure. Check 80 F3 DOD BOD F4 X MacBook Air : □ 0* 1/5 Julianna ? 000 Ar 2024 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility F12 F8 FIOarrow_forwardPLEASE ANSWER QUESTION IN 15 MINTUES NOT MORE PLEASE AND THANK YOU. If you do answer the question correctly and post it in the next 15 minutes, NO NEED TO SHOW THE WORK, I JUST WOULD LIKE THE CORRECT ANSWER AS SOON AS POSSIBLE. isnt the answer e)none of theses since the correct : Structural Isomers Optical isomers are the compounds which has the same number of atoms and bonds, but different type of spatial arrangement of bonds. The compounds as these isomers are non-superimposable mirror images of each other. Structural isomers are the constitutional isomers in which two compounds has same molecular formula but different structures. Stereoisomer are the compounds which have same number of atoms and bonds but differs by their spatial arrangement of atoms . Optical isomers are a type of stereo isomers. Geometric isomers are the isomers which has same number of atoms and even same structural formula but these compounds differ in the arrangement of bonds. For example :…arrow_forwardPlease correct answer and don't use hand ratingarrow_forward
- Can you please explain what this asking for ?arrow_forwardSubject : chemarrow_forwardFörčé Completion This test can be saved and resumed at any pc Remaining Time: 58 minutes, 20 seconds. Question Completion Status: A Moving to another question will save this response. Question 5 Draw at least 5 isomers for C5H11C1? Attach File Browse My Computer A Moving to another question will save this response.arrow_forward
- List answer using letters not structures. Thank you!arrow_forwardQuestion 20 A carbohydrate can be defined as a molecule O whose name ends in "-ase". composed of carbon atoms bonded to water molecules. O composed of amine groups and carboxylic acid groups bonded to a carbon skeleton. that is an aldehyde or ketone and that has more than one hydroxyl group. O composed mostly of hydrocarbons and soluble in non-polar solvents. Question 21arrow_forward19. Draw the structure for the compound at the bottom of the page. Show your reasoning. C3H1403 100 80 4880 3580 3000 2568 2000 1500 1000 2H 3H 3H 2H 2H 2H 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 PPM 9LC42 86 9 1745.80 BL SS LIC 1486.89 1387. 12 852.85 O 208arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning

Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning