![Glencoe Chemistry: Matter and Change, Student Edition](https://www.bartleby.com/isbn_cover_images/9780076774609/9780076774609_smallCoverImage.jpg)
(a)
Interpretation:
Amino acid from Table 23.1 should be classified into each of the categories nonpolar v. polar.
Concept introduction:
Proteins are
They polymerize by peptide linkage to form dipeptide, oligopeptide and polypeptide molecules. Each peptide bond formation is a condensation reaction that occurs with the elimination of water molecule.
![Check Mark](/static/check-mark.png)
Answer to Problem 6SSC
Glycine, valine and phenylalanine are nonpolar amino acids and, serine, cysteine, lysine, glutamic acid, glutamine are polar amino acids.
Explanation of Solution
Polar amino acid is directed towards the outside of the protein because of the hydrophilic properties of side chain whereas the nonpolar amino acid is directed towards the inside of protein (R group repelled by water) because of the hydrophobic nature.
The given amino acids are: Glycine, Serine, Cysteine, Lysine, Glutamic acid, Glutamine, Valine and Phenylalanine.
The structure of Glutamine is:
The structure of serine is:
The structure of Cysteine is:
The structure of Lysine:
The structure of glutamic acid:
The structure of Glycine is:
The structure of valine is:
The structure of phenylalanine is:
Glycine is nonpolar as it is neutral species; also nonpolar hydrogen is linked as shown below:
Valine is nonpolar as it is neutral species; also nonpolar group is linked as shown below:
Serine is polar amino acid as it consists of polar R group:
Cysteine is polar amino acid as it consists of polar R group:
Glutamine is a polar amino acid as it consists of polar R group:
Lysine is a polar amino acid as it consists of polar R group:
Glutamic acid is a polar amino acid as it consists of polar R group:
Phenylalanine is nonpolar as it is neutral species; also nonpolar group is linked as shown below:
Therefore; glycine, valine and phenylalanine are nonpolar amino acids and, serine, cysteine, lysine, glutamic acid, glutamine are polar amino acids.
(b)
Interpretation:
Amino acid from Table 23.1 should be classified into each of the categories aromatic v. aliphatic.
Concept introduction:
Proteins are polymeric biomolecules which are formed by the polymerisation of amino acids. Amino acids are the organic molecules with
They polymerize by peptide linkage to form dipeptide, oligopeptide and polypeptide molecules. Each peptide bond formation is a condensation reaction that occurs with the elimination of water molecule.
![Check Mark](/static/check-mark.png)
Answer to Problem 6SSC
The amino acids which are aliphatic in nature are glycine, serine, cysteine, lysine, glutamic acid, glutamine, valine whereas the amino acid which is aromatic.
Explanation of Solution
A cyclic ring structure which contains carbon atoms and hydrogen atoms is known as aromatic ring and the compound which has aromatic ring is known as
The compound which consists of carbon and hydrogen linked with each other either in a straight chain, branched chain and non-aromatic rings is known as aliphatic compounds.
The given amino acids are: Glycine, Serine, Cysteine, Lysine, Glutamic acid, Glutamine, Valine and Phenylalanine.
The structure of Glutamine is:
The structure of serine is:
The structure of Cysteine is:
The structure of Lysine:
The structure of glutamic acid:
The structure of Glycine is:
The structure of valine is:
The structure of phenylalanine is:
According to above structures, the amino acids which are aliphatic in nature are glycine, serine, cysteine, lysine, glutamic acid, glutamine, valine as these amino acids contain carbon and hydrogen bonds (hydrocarbon) whereas the amino acid which is aromatic is phenylalanine as it contains aromatic ring in its side chain.
(c)
Interpretation:
Amino acid from Table 23.1 should be classified into each of the categories acidic v. basic.
Concept introduction:
Proteins are polymeric biomolecules which are formed by the polymerisation of amino acids. Amino acids are the organic molecules with
They polymerize by peptide linkage to form dipeptide, oligopeptide and polypeptide molecules. Each peptide bond formation is a condensation reaction that occurs with the elimination of water molecule.
![Check Mark](/static/check-mark.png)
Answer to Problem 6SSC
Lysine and Glutamic acid is basic and acidic amino acid. The remaining amino acids are neutral.
Explanation of Solution
The amino acids which contain R group as a
The amino acids which contain R group as a
The given amino acids are: Glycine, Serine, Cysteine, Lysine, Glutamic acid, Glutamine, Valine and Phenylalanine.
The structure of Glutamine is:
Glutamine is neither acidic nor basic as the side chain of glutamine is uncharged (polar R group). Thus, glutamine is a neutral amino acid.
The structure of serine is:
Serine is neither acidic nor basic as the side chain of serine is uncharged (polar R group). Thus, serine is a neutral amino acid.
The structure of Cysteine is:
Cysteine is neither acidic nor basic as the side chain of cysteine is uncharged (polar R group). Thus, cysteine is a neutral amino acid.
The structure of Lysine:
Lysine is basic in nature as the side chain of lysine consists of amine group. Thus, lysine is a basic amino acid.
The structure of glutamic acid:
Glutamic acid is acidic in nature as the side chain of glutamic acid consists of carboxylic group. Thus, Glutamic acid is an acidic amino acid.
The structure of Glycine is:
Glycine is neither acidic nor basic as the side chain of glycine is uncharged (polar R group). Thus, glycine is a neutral amino acid.
The structure of valine is:
Valine is neither acidic nor basic as the side chain of valine is uncharged (polar R group). Thus, valine is a neutral amino acid.
The structure of phenylalanine is:
Phenylalanine is neither acidic nor basic as the side chain of phenylalanine is uncharged (polar R group). Thus, phenylalanine is a neutral amino acid.
Chapter 23 Solutions
Glencoe Chemistry: Matter and Change, Student Edition
Additional Science Textbook Solutions
Organic Chemistry (8th Edition)
Genetic Analysis: An Integrated Approach (3rd Edition)
Chemistry: Structure and Properties (2nd Edition)
Applications and Investigations in Earth Science (9th Edition)
Campbell Essential Biology (7th Edition)
Biology: Life on Earth (11th Edition)
- Gas Law Studies 1. Mass of zinc Determination of 0.899 2) Moles of zinc 0.01361 mol 3.) Moles of hydrogen 00? ← I was told to calculate this number from mole of zinc. 350m So does that mean it will be 0.01361 mol too? 4 Volume of water collected (mL) 5) VL of water collected (Liters) 0.350 L 6) Temp of water collected (°C) 7) Temp of water collected (°K) 8) Atmospheric pressure (mm) 9) Vapor pressure of water (mm) 10) Corrected pressure of hydrogen 20% 29°C 764.0mm Hg (mm) 17.5mm 11) Corrected pressure of hydrogen (atm) 12) Experimentally calculated value of 19 13. Literature value of R 14) % Error 15) Suggest reasons for the % error (#14)arrow_forwardNo wedge or dashes. Do proper structure. Provide steps and explanation.arrow_forward10 Question (1 point) Draw curved arrow notation to indicate the proton transfer between NaOH and CH3CO₂H. 2nd attempt :0- H See Periodic Table See Hint Draw the products of the proton transfer reaction. Don't add a + sign between the products.arrow_forward
- Nonearrow_forward4. Experimental Procedure. a. How many (total) data plots are to be completed for this experiment? Account for each. b. What information is to be extracted from each data plot?arrow_forwardProvide the IUPAC name of the following molecule. Don't forget to include the proper stereochemistry where appropriate.arrow_forward
- 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
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)