Campbell Biology in Focus
3rd Edition
ISBN: 9780134710679
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Rebecca Orr
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 3.1, Problem 4CC
Summary Introduction
To draw:
The structure where, from a cysteine molecule, the NH2 group is replaced with a COOH (carboxyl) group. Also, determine how this change would alter the chemical properties and state whether the central carbon atomis asymmetric after or before the alteration.
Concept introduction:
Amino acids are the molecules that are organic and consist of both the carboxyl and amino groups.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Draw the structures of L-Cysteine from highly protonated to depronated form. Note Structure A as the most protonated form. Provide the charge of each structure.
(Answer structure A and B pls)
The figure below illustrates the molecular structures of two fatty acids.
A
B
H₂C
The structural formula of erucic acid and behenic acid
с
H₂C
D
erucic acid
behenic acid
Which of the following best explains why erucic acid is liquid at room temperature but behenic acid is solid at
room temperature?
O
OH
The presence of a double carbon to carbon bond in erucic acid prevents the molecule
from packing closely together.
The lack of any double carbon-carbon bonds in behenic acid causes the molecule to be
come polar and therefore packed more tightly.
The larger number of carbon atoms in erucic acid prevents the molecule from packing
tightly together.
OH
The smaller number of carbon atoms in behenic acid creates stronger covalent bonds
between the carbon atoms allowing for them to pack more tightly together.
Consider the following Newman projection:
CH3
Br
CH3
Br
Br
What word or two-word phrase describes this conformation?
How many Br atoms are eclipsed by the CH3 group on the front carbon?
How many CH3 groups are gauche to the CH3 group on the front carbon?
How many Br atoms are anti to the CH3 group on the front carbon?
☐
☐
☐
Chapter 3 Solutions
Campbell Biology in Focus
Ch. 3.1 - How are gasoline and fat chemically similar?Ch. 3.1 - Which molecules in Figure 3.4a re isomers? For...Ch. 3.1 - Prob. 3CCCh. 3.1 - Prob. 4CCCh. 3.2 - How many molecules of water are needed to...Ch. 3.2 - WHAT IF? Suppose you eat a serving of fish. What...Ch. 3.3 - Write the formula for a monosaccharide that has...Ch. 3.3 - A dehydration reaction joins two glucose molecules...Ch. 3.3 - WHAT IF? After a cow is given antibiotics to treat...Ch. 3.4 - Compare the structure of a fat (triglyceride) with...
Ch. 3.4 - Why are human sex hormones considered lipids?Ch. 3.4 - Prob. 3CCCh. 3.5 - Why does a denatured protein no longer function...Ch. 3.5 - What parts of a polypeptide participate in the...Ch. 3.5 - WHAT IF? Where would you expect a polypeptide...Ch. 3.6 - DRAW IT Go to Figure 3.27a and, for the top three...Ch. 3.6 - Prob. 2CCCh. 3.7 - How would sequencing the entire genome of an...Ch. 3.7 - Given the function of DNA, why would you expect...Ch. 3 - Which functional group is not present in this...Ch. 3 - MAKE CONNECTIONS Which chemical group is most...Ch. 3 - Prob. 3TYUCh. 3 - Which of the following statements concerning...Ch. 3 - Prob. 5TYUCh. 3 - The structural level of a protein least a fleeted...Ch. 3 - Enzymes that break down DNA catalyze the...Ch. 3 - Prob. 8TYUCh. 3 - The molecular formula for glucose is C6H12O6. What...Ch. 3 - Construct a table that organizes the following...Ch. 3 - Prob. 11TYUCh. 3 - Prob. 12TYUCh. 3 - FOCUS ON ORGANIZATION Proteins, which have diverse...Ch. 3 - Prob. 14TYUCh. 3 - SYNTHESIZE YOUR KNOWLEDGE Given that the function...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- DRAW IT Suppose you had an organic molecule suchas cysteine (see Figure 4.9, sulfhydryl group example),and you chemically removed the —NH2 group andreplaced it with —COOH. Draw this structure. Howwould this change the chemical properties of themolecule? Is the central carbon asymmetric beforethe change? After?arrow_forwardA victim approaches you and says "Please help me! I was kidnapped by a molecule. The suspect is either CH2NH or CH3NH2. Use this information to solve the three parts in the imagearrow_forwardThe surface of the eye is wet by tears, and to minimize evaporation, the tear layer is coated with lipids. One of these lipids is built from oleic acid and a 32-carbon fatty acid that has a double bond between carbons 9 and 10 and a hydroxyl group attached to the omega carbon. The carboxyl group of oleic acid condenses with the hydroxyl group in the longer lipid. Draw the structure of the reaction product. It’s OK to draw a condensed structure.arrow_forward
- When a substance such as sodium chloride is dissolved in water, the ions become completely surrounded by water molecules, forming structures called hydration spheres. When the sodium salt of a fatty acid is mixed with water, the carboxylate group of the molecule becomes hydrated, but the hydrophobic portion of the molecule is poorly hydrated, if at all. Using a circle to represent the carboxylate group and an attached squiggly line to represent the hydrocarbon chain of a fatty acid, draw a picture of how fatty acids interact with water.arrow_forwardThe chemical structure of food coloring and oil are not provided on their packaging, but based on the results of these experiments you can predict what you might see. Explain whether you think there are more -OH (hydroxyl) groups or -CH hydrocarbon chains on a molecule of food coloring and on an oil moleculearrow_forwardObserve the structures of glucose and fructose in figure shown. These two molecules are H. H-C-OH Н—С—он C=0 но-с—н HO-C-H H-C-OH H-C-OH H-C-OH H-C-OH H-C-OH H-C-OH H H. glucose fructose A. geometric isotopes. B. enantiomers. C. stereoisomers. D. structural isomers.arrow_forward
- Draw all three staggered conformations for the following compound, viewed along the C₂-C3 bond. Determine which conformation is the most stable, taking into account gauche interactions and hydrogen-bonding interactions. (J. Phys. Chem. A 2001, 105, 6991-6997) Provide a reason for your choice by identifying all of the interactions that led to your decision. H H&COH C₂ C3 HỌ CH CH3 Which of the following is the most stable staggered conformer? Me H OH Me OH Me- Me Me H Conformer A OH OH OH HO H H H Conformer B Conformer C Me Conformer B because the anti OH groups avoid hydrogen bonding, which is a destabilizing effect. Conformer A because there are only two gauche interactions, and hydrogen bonding between the two OH groups is a stabilizing effect. Conformer C because there is no steric strain for Me-OH gauche interactions and hydrogen bonding between the two OH groups is a stabilizing effect. Conformer B because the large OH groups are anti to each other.arrow_forwardH HOH -он HOH H FOH но- но- -H- HO,arrow_forward72. Use Figure 2 to answer the following questions. (1.4) KU HOCH, OH C3 H C H С — H ОН ОН ribose Figure 2 (a) Which type of molecule does this diagram represent? (b) What is the chemical formula for this molecule? of macromolecules does this (c) What group molecule belong to? エーO エ-Oarrow_forward
- A B CH₂OH H H OH E Which carbon is the anomeric carbon in the structure shown here? OH H OH CH₂OH Question 15 of 25 D A) A B) B C) C D) D E) E Submitarrow_forwardWhen a substance such as sodium chloride is dissolved inwater, the ions that form become completely surrounded bywater molecules, which form structures called hydrationspheres. When the sodium salt of a fatty acid is mixed withwater, the carboxylate group of the molecule becomeshydrated but the hydrophobic hydrocarbon portion of themolecule is poorly hydrated, if at all. Using a circle torepresent the carboxylate group and an attached squigglyline to represent the hydrocarbon chain of a fatty acid, drawa picture of how fatty acids interact in water.arrow_forwardFor the following lipid, answer the questions listed below. 0- HC-o (CH)),CH=CH(CH,);CH; H,C-o-c-(CH2);CH=CHCH,CH=CHỊCH,),CH, Is this lipid considered a fat or oil? a. b. How many H2 molecules would be needed to go through a complete hydrogenation reaction? Would the hydrogenated product (after hydrogenation has occurred) have a higher or lower mp than the original starting material? С.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Human Biology (MindTap Course List)BiologyISBN:9781305112100Author:Cecie Starr, Beverly McMillanPublisher:Cengage LearningBiology (MindTap Course List)BiologyISBN:9781337392938Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. BergPublisher:Cengage Learning
Human Biology (MindTap Course List)
Biology
ISBN:9781305112100
Author:Cecie Starr, Beverly McMillan
Publisher:Cengage Learning
Biology (MindTap Course List)
Biology
ISBN:9781337392938
Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
Publisher:Cengage Learning