Concept explainers
(a)
To determine: The basic and non-basic nitrogen atoms of the histidine heterocycle.
Interpretation: The basic and non-basic nitrogen atoms of the histidine heterocycle are to be predicted.
Concept introduction: An amino acid that consists of
(b)
To determine: The reason corresponding to the fact that the protonated form of histidine is a particularly stable cation with help of resonance forms.
Interpretation: The reason corresponding to the fact that the protonated form of histidine is a particularly stable cation with help of resonance forms are to be predicted.
Concept introduction: An amino acid that consists of
(c)
To determine: The structures of histidine that shows histidine accepts a proton on the basic nitrogen of the heterocycle and then get deprotonated on the other heterocyclic nitrogen and the explanation regarding the fact that the histidine might function as a pipeline to transfer protons between sites within an enzyme and its substrate.
Interpretation: The structures of histidine that shows histidine accepts a proton on the basic nitrogen of the heterocycle and then get deprotonated on the other heterocyclic nitrogen are to be shown and the explanation regarding the fact that histidine might function as a pipeline to transfer protons between sites within an enzyme and its substrate is to be stated.
Concept introduction: An amino acid that consists of
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Chapter 24 Solutions
EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
- K m Choose the best reagents to complete the following reaction. L ZI 0 Problem 4 of 11 A 1. NaOH 2. CH3CH2CH2NH2 1. HCI B OH 2. CH3CH2CH2NH2 DII F1 F2 F3 F4 F5 A F6 C CH3CH2CH2NH2 1. SOCl2 D 2. CH3CH2CH2NH2 1. CH3CH2CH2NH2 E 2. SOCl2 Done PrtScn Home End FA FQ 510 * PgUp M Submit PgDn F11arrow_forwardNonearrow_forwardPlease provide a mechanism of synthesis 1,4-diaminobenzene, start from a benzene ring.arrow_forward
- Consider this step in a radical reaction: Br N O hv What type of step is this? Check all that apply. Draw the products of the step on the right-hand side of the drawing area below. If more than one set of products is possible, draw any set. Also, draw the mechanism arrows on the left-hand side of the drawing area to show how this happens. O primary Otermination O initialization O electrophilic O none of the above × ☑arrow_forwardNonearrow_forwardCan I get a drawing of what is happening with the orbitals (particularly the p orbital) on the O in the OH group? Is the p orbital on the O involved in the ring resonance? Why or why not?arrow_forward
- 1) How many monochlorination products-including stereochemistry- are there for the molecule below:arrow_forwardSelect an amino acid that has and N-H or O-H bond in its R-group (you have 8 to choose from!). Draw at least two water molecules interacting with the R-group of the amino acid.arrow_forwardIs this aromatic?arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
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