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Concept explainers
a.
To identify:
The N and C terminus of the given peptides. Phe-Glu.
Introduction:
The condensation reaction between the N-terminal of one amino acid and carboxylic group of another amino acid leads to the formation of a peptide bond. According to the convention, N-terminal of amino acid in a peptide bond is written on the left hand side while the C-terminal of amino acids is written on the right hand side.
The N-terminus represents the starting of the polypeptide which refers the free amino group and the C-terminus represents the end of the polypeptide which refers the free carboxyl group.
b.
To identify:
The N and C terminus of the given peptides KCG.
Introduction:
The condensation reaction between the N-terminal of one amino acid and carboxylic group of another amino acid leads to the formation of a peptide bond. According to the convention, N-terminal of amino acid in a peptide bond is written on the left hand side while the C-terminal of amino acids is written on the right hand side.
The N-terminus represents the starting of the polypeptide which refers the free amino group and the C-terminus represents the end of the polypeptide which refers the free carboxyl group.
c.
To identify:
The structural formula for the given peptide His-Met-Gln.
Introduction:
The condensation reaction between the N-terminal of one amino acid and carboxylic group of another amino acid leads to the formation of a peptide bond. According to the convention, N-terminal of amino acid in a peptide bond is written on the left hand side while the C-terminal of amino acids is written on the right hand side.
The N-terminus represents the starting of the polypeptide which refers the free amino group and the C-terminus represents the end of the polypeptide which refers the free carboxyl group.
d.
To determine:
The structural formula for the given peptide WY.
Introduction:
The condensation reaction between the N-terminal of one amino acid and carboxylic group of another amino acid leads to the formation of a peptide bond. According to the convention, N-terminal of amino acid in a peptide bond is written on the left hand side while the C-terminal of amino acids is written on the right hand side.
The N-terminus represents the starting of the polypeptide which refers the free amino group and the C-terminus represents the end of the polypeptide which refers the free carboxyl group.
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Chapter 10 Solutions
General, Organic, and Biological Chemistry (3rd Edition)
- Nonearrow_forwardH2SO4 (cat.), H₂O 100 °C NH₂arrow_forwardX Draw the major products of the elimination reaction below. If elimination would not occur at a significant rate, check the box under the drawing area instead. ది www. Cl + OH Elimination will not occur at a significant rate. Click and drag to start drawing a structure.arrow_forward
- Nonearrow_forward1A H 2A Li Be Use the References to access important values if needed for this question. 8A 3A 4A 5A 6A 7A He B C N O F Ne Na Mg 3B 4B 5B 6B 7B 8B-1B 2B Al Si P 1B 2B Al Si P S Cl Ar K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe * Cs Ba La Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn Fr Ra Ac Rf Ha ****** Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr Analyze the following reaction by looking at the electron configurations given below each box. Put a number and a symbol in each box to show the number and kind of the corresponding atom or ion. Use the smallest integers possible. cation anion + + Shell 1: 2 Shell 2: 8 Shell 3: 1 Shell 1 : 2 Shell 2 : 6 Shell 1 : 2 Shell 2: 8 Shell 1: 2 Shell 2: 8arrow_forwardNonearrow_forward
- IV. Show the detailed synthesis strategy for the following compounds. a. CH3CH2CH2CH2Br CH3CH2CCH2CH2CH3arrow_forwardDo the electrons on the OH participate in resonance with the ring through a p orbital? How many pi electrons are in the ring, 4 (from the two double bonds) or 6 (including the electrons on the O)?arrow_forwardPredict and draw the product of the following organic reaction:arrow_forward
- Nonearrow_forwardRedraw the molecule below as a skeletal ("line") structure. Be sure to use wedge and dash bonds if necessary to accurately represent the direction of the bonds to ring substituents. Cl. Br Click and drag to start drawing a structure. : ☐ ☑ Parrow_forwardK 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_forward
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