![EBK GENERAL, ORGANIC, AND BIOLOGICAL CH](https://www.bartleby.com/isbn_cover_images/8220100853180/8220100853180_largeCoverImage.jpg)
Concept explainers
Interpretation:
The one which is a representation of sec-butyl group has to be chosen from the given options.
Concept Introduction:
Alkyl groups are named according to
Rule 1:
Longest continuous chain which begins at the point of attachment of the alkyl group becomes the base name for the alkyl group.
Rule 2:
Base chain that is identified is numbered in a way beginning at the point of attachment.
Rule 3:
The substituents that are present in the base chain is listed in alphabetical order using the locant as prefixes whenever necessary.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 12 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- Consider the tripeptide phenylalanylcysteyl methionine. Part: 0 / 2 Part 1 of 2 Draw the structure of this tripeptide at physiological pH. Click and drag to start drawing a structure. : ☐arrow_forwardAs the image asks, which of these is L-isoleucine?arrow_forwardComplete the following table by providing the Fischer and Haworth Projections of the given sugars. In the Fischer Projection put an asterisk (*) mark in the chiral centers of the molecule. Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer D-Mannose D-Xylose L-Lyxosearrow_forward
- Which of the following statements are TRUE? Multiple answers:Multiple answers are accepted for this question PLEASE SHOW WORK FOR EACH PART AND EXPLAIN WHY EACH ANSWER CHOICE IS WRONG OR RIGHT a. The tripeptide His-Lys-Glu has a net charge of -2 at pH 8.0. b. The tripeptide Asp-Asp-Asp has a net charge of -3 at pH 7.0. c. The tetrapeptide His-His-His-His has a net charge of -1 at pH 7.0. d. There are 6 possible sequences for a tripeptide containing Arg - His - and Pro. e. Certain bacteria synthesize cyclic tetrapeptides. The net charge at pH 7.0 of a cyclic tetrapeptide consisting of two Pro and two Tyr is 0.arrow_forwardSerine is an uncharged, polar amino acid (below and left). Threonine (below and right) is another uncharged, polar amino acid. Illustrate the hydrolysis of a dipeptide that was made from these two amino acids. Be sure to write all involved reactants and products in the structural form like Serine, and as a proper chemical equation; eg. reactant(s) – product(s). Your diagram of the dipeptide must show the N-terminal and C-terminal ends at opposite sides of the dimer molecule, and you need to indicate where the peptide bond is with an arrow/highlighter. 2. H C-N OH NH, но CH, CH,-CH -C-COOH онarrow_forwardWhy is the formation of a peptide bond called a condensation reaction? Explain brieflyarrow_forward
- Column A shows the names of some of the c functional groups. Column B shows their structure. Match each entry in column A one in column B.arrow_forwardShow the complete steps and products of the Haworth Projection structure of the following saccharides. The males have to answer the structure of D-sorbose and the females are the structure of D-mannose. (ANSWER ALL)arrow_forwardWould you consider the formation of a peptide bond to be an example of a neutralization reaction? Explain your reasoning. 1. *arrow_forward
- Of the 20 protein-derived amino acids shown in Table 27.1, how many contain Q.) an aromatic ringarrow_forwardFollowing are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses. Identify the pairs that are enantiomers. CHO сно H-C- OH H-C-OH H-C- OH но-с — н н-с—он но- ČHOH ČH,OH сно CHO Н-с—он но—с— н H-C- OH H-C-OH но—с—н Н-с—он ČHOH ČH,OH сно сно н-с—он но—с —н но—с— н но -с — н H-C- OH но- C-H ČH,OH ČH,OHarrow_forwardWhat are the structural differences between bilirubin and urobilin? (Select all that apply.) O Ring is opened in the first compound, but is not in the second compound. Several methylene bridges are reduced in the second compound. O Iron atom is absent in the second compound, but is present in the first compound. The central methylene bridge is reduced in the second compound, but is not in the first compound. O Ring is opened in the second compound, but is not in the first compound. Some vinyl groups are reduced into ethyl groups in the second compound. The central methylene bridge is oxidised in the second compound, but is not in the first compound. O Some vinyl groups are reduced into ethyl groups in the first compound.arrow_forward
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education
![Text book image](https://www.bartleby.com/isbn_cover_images/9780134580999/9780134580999_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781947172517/9781947172517_coverImage_Textbooks.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259398629/9781259398629_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780815344322/9780815344322_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781260159363/9781260159363_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781260231700/9781260231700_smallCoverImage.gif)