FOUNDATIONS OF COLLEGE CHEM +KNEWTONALTA
FOUNDATIONS OF COLLEGE CHEM +KNEWTONALTA
15th Edition
ISBN: 9781119797807
Author: Hein
Publisher: WILEY
Question
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Chapter 20.4, Problem 20.4P

(a)

Interpretation Introduction

Interpretation:

Full name of Pro-Tyr has to be written.

Concept Introduction:

Amino acids are compounds that contain an amino group and carboxyl group in it.  The carboxyl carbon atom is the C1 carbon atom.  Amino acids combine together by condensation reaction resulting in formation of a peptide linkage.  If two amino acids combine to form a peptide linkage, the formed compound is known as dipeptide.  The peptides are named considering the amino acids present in it.  Peptides are named simply as acyl derivatives of the amino acid present in C-terminal.  The N-terminal amino acids is named by replacing the suffix “-ine” with “-yl” and the C-terminal amino acid name is given as such.

(b)

Interpretation Introduction

Interpretation:

Full name of Gln-His-Leu has to be written.

Concept Introduction:

Refer part (a).

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#1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un- cyclize. Undo the ring into all possible molecules. (2pts, no partial credit) hv
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I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."

Chapter 20 Solutions

FOUNDATIONS OF COLLEGE CHEM +KNEWTONALTA

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