
Concept explainers
Interpretation: The types of interactions that occur in the given amino acids to maintain their tertiary structure are to be stated.
Concept introduction: Amino acids are the building blocks of proteins. They bind together to form large chain molecules of high molecular masses known as proteins. Aliphatic and
To determine: The type of interaction that occurs between the side chains of the given amino acids.

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Chapter 21 Solutions
Bundle: Chemistry: An Atoms First Approach, 2nd, Loose-Leaf + OWLv2, 4 terms (24 months) Printed Access Card
- For the mechanism, show everything, lone paires, charges and arrow pleasearrow_forwardmolecule 0= OH ☐ ☐ type of molecule (check all that apply) fatty acid monoglyceride diglyceride triglyceride saturated unsaturated monounsaturated ☐ polyunsaturated ☐ ☐ ☐ ☐ ☐ 010 0 0 0 0 0 0 ☐ ☐ ☐ ☐☐☐☐ U omega-3 omega-6 fatty acid monoglyceride diglyceride triglyceride saturated unsaturated monounsaturated polyunsaturated omega-3 omega-6 fatty acid monoglyceride diglyceride triglyceride saturated unsaturated monounsaturated polyunsaturated omega-3 omega-6 OH OHarrow_forward'☐ : ☑ ด Suppose an alien life form has DNA just like human DNA remain the same.) - except that the alien DNA is made from deoxyarabinose instead of deoxyribose. (All other ingredients Draw the structure of a nucleotide containing thymine from which the alien DNA would be assembled. Note: be sure to draw the molecule as it would exist at physiological pH. Click and drag to start drawing a structure.arrow_forward
- Predict the products of the following biochemical reaction: CH2 CH-O + 3 KOH CH2-0 In particular, draw the structure of the product or products P in the drawing area below. If there are no products, because this reaction won't happen, check the No reaction box under the drawing area. Note: if there is more than one product, you can draw them in any arrangement you like. Also, just draw the structure of each product. You don't have to draw the complete right-hand side of the equation, including stoichiometric coefficients. No reaction Click and drag to start drawing a structure. : 5 èarrow_forwardAssign these spectrumarrow_forwardIf I have 30% H2O2, indicate how to prepare a 6% H2O2 solution.arrow_forward
- 7) 8) FCI II -C-C-C=C-C || Br Br || -C=C-Br -CEC-C-C- 10) 11) F Br i OH مله 12) Br i 13) 14) 15) CH3CHFCHFC=CH C(OH)Br2CHF(CH2)4CH2CH3 CH3(CH2)3CH=CH(CH2)2CH3arrow_forwardName 1) 3-fluoro, 1-butene 2) 2-heptene 2,3-difluoro- 1-pentene 4) 6-iodo,4-methyl- 2-decyne 5) 4,4-dibromo- 1,2-butandiol Complete structural formula F -C=C-C-C- Line formula Condensed structural formula N F CH2=CHCHFCH3arrow_forward1. Part 1: Naming Organic Compounds он H₁C-C-CH3 CH3 Br CI CI 2. Br-CH-CH-CH₂ H₂C-CH-C= -CH-CH2-CH3 3. HC-CH-CH-C-OH 5. H₂C-CH-CH₂-OH 7. OH 4. CH CH₂-CH₂ 6. сно CH-CH-CH-CH₂-CH₂ H₁₂C-CH-CH-CH-CH₁₂-CH₁₂ 8. OHarrow_forward
- 11 Organic Chemistry Organic Nomenclature Practice Name/Functional Group n-butane Formula Structural Formula (1) C4tt10 H3C C- (2) CH3CH2CH2 CH 3 H₂ -CH3 Н2 name & functional group (1) and (2) OH H₁₂C Н2 name only (1) and (2) name only (1) and (2) H₁C - = - CH₂ Н2 HC=C-C CH3arrow_forwardUnder aqueous basic conditions, nitriles will react to form a neutral organic intermediate 1 that has an N atom in it first, and then they will continue to react to form the final product 2: NC H₂O он- H₂O 1 2 OH Draw the missing intermediate 1 and the final product 2 in the box below. You can draw the two structures in any arrangement you like. Click and drag to start drawing a structure.arrow_forwardAssign these COSY Spectrumarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningWorld of ChemistryChemistryISBN:9780618562763Author:Steven S. ZumdahlPublisher:Houghton Mifflin College Div





