
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

Want to see the full answer?
Check out a sample textbook solution
Chapter 24 Solutions
Student's Solutions Manual for Organic Chemistry
- Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. (CH3)2NH, TSOH Drawingarrow_forwardSo, the first image is what I'm trying to understand regarding my approach. The second image illustrates my teacher's method, and the third image includes my notes on the concepts behind these types of problems.arrow_forwardHAND DRAWarrow_forward
- Draw a mental model for calcium chloride mixed with sodium phosphatearrow_forwardhere is my question (problem number 20) please explain to me thanks!arrow_forwardThe bromination of anisole is an extremely fast reaction. Complete the resonance structures of the intermediate arenium cation for the reaction (Part 1), and then answer the question that follows (Part 2).arrow_forward
- Drawing of 3-fluro-2methylphenolarrow_forwardWhich compound(s) will be fully deprotonated (>99%) by reaction with one molar equivalent of sodium hydroxide? I, II, III I, || I, III I only II, III SH | H3C-C=C-H || III NH2arrow_forwardWill NBS (and heat or light) work for this reaction, or do we have to use Br2?arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
