The image depicts a molecular structure diagram of a polypeptide segment. Key functional groups in the structure include alpha carbon, R groups, and peptide bonds. The instructional text at the top reads:"Drag the appropriate labels to their respective targets. Labels can be used more than once."To the left, there is a list of labels:- α carbon- R group- peptide bondThe molecular diagram in the center shows a sequence of amino acids with highlighted areas meant for label placement. Chemical groups include:1. An amino group $(\text{H}_3\text{N}^+\text{--CH--CO--NH--CH}_2)$ with a phenol ring as an R group.2. A central carbon marked with potential label boxes.3. Peptide bonds between amino acids shown as $\text{C--NH--CH}$ links.4. Several side chains indicating different R groups: - A phenyl ring with an OH group. - A group with $\text{CH}_2\text{OH}$. - A group with $\text{CH}_2(\text{CH}_2)_2\text{NH}_3^+$.The structure involves typical peptide bonds linking amino acids and a variety of side chains characteristic of different R groups in proteins.The bottom of the diagram has 'Reset' and 'Help' buttons, suggesting an interactive component for educational purposes.

Given molecule is peptide. Which formed by peptide bond . From alpha amino acids. Peptide bond is…

Drag the appropriate labels to their respective targets. Labels can be used more than once. Reset Help a carbon HÑ-CH- -NH-CH-Č NH-CH CH2 CH,OH R group peptide bond OH 梦 $ * 4:19 PM 71F A G E D 40 10/10/20 立

Drag the appropriate labels to their respective targets. Labels can be used more than once. Reset Help a carbon HÑ-CH- -NH-CH-Č NH-CH CH2 CH,OH R group peptide bond OH 梦 $ * 4:19 PM 71F A G E D 40 10/10/20 立

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Which structure below contains a peptide bond? H H2N FHÇ HO- CH3 O CH3 H2N -CH- CFOH CH3 H2N -CH2- --O NH CH3
Classify the following amino acids as highlight whichever is correct Neutral/ non-polar/ acidic/ basic
21. The melting points (mp) of three beta agonist homologues are given below OH HO OH Terbutaline mp 119-122°C OH zey HO. OH Metaproterenol mp 100°C НО. HO OH H N Isoproterenol mp 155.5°C What is their expected order of solubility in water, from lowest to highest? A. Terbutaline>metaproterenol>isoproterenol B. Metaproterenol>terbutaline>isoproterenol C. Isoproterenol>metaproterenol>terbutaline D. Isoproterenol>terbutaline>metaproterenol E. Metaproterenol>isoproterenol>terbutaline 26. The melting point of isosorbide-2,5-diaspirinate is higher than that of aspirin. What is the significance of higher melting point in preformulation? A. High melting point is generally associated with low aqueous solubility B. High melting point is generally associated with high aqueous solubility C. Melting point is inversely proportional to density D. Melting point is used in the calculation of viscosity E. A high melting point indicates better chemical and physical stability in aqueous solution
What is the single-letter code of the primary sequence for our favorite peptide below? OH NH₂ NH₂ HO HO HN NH NH₂ OH
Check the box under each a amino acid. If there are no a amino acids at all, check the "none of them" box under the table. Note for advanced students: don't assume every amino acid shown must be found in nature. NH, Ô H3N-CH-COO HO-C C-H H₂N CH3-CH OH CH2 0 C=O 0 O C=O சீசீ 0 HO CH3 H3N-CH-COO CH-CH3 CH3-CH H3N-C-COO CH2 H OH O O Onone of them Explanation Check 0 OH CH2 CH3-CH H₂N C-COOH H O $ % 2 2 3 4 5 6 a W E R & 7 HI
Following is the structure of a peptide with the name seryllysylaspartate. What is the amino acid at the N-terminus of this peptide? NH3 CH₂ 0 | CH₂ | CH₂ | CH, O || OH I CH, O || C | CH, O || H₂N-C-C-N-C-C-N-C-C-O I H | I | | HH HH O seryllysine O aspartate O lysine O serine 0=
I need help with predicting the ester.
.
Is peptide bond 2 (colored red) drawn cis or trans? O trans O cis NH₂ SH NH 1 01 OH HN CH3 OH
Show how to convert the side-chain carboxyl group to a benzyl ester using benzyl chloride as a source of the benzyl group.
Please don't provide handwriting solution
Only typed solution