Amino Acids Glycine is the smallest of the amino acids. It is ambivalent‚ meaning that it can be inside or outside of the protein molecule. In aqueous solution at or near neutral pH‚ glycine will exist predominantly as the zwitterion. Alanine is a hydrophobic molecule. It is ambivalent‚ meaning that it can be inside or outside of the protein molecule. The α carbon of alanine is optically active; in proteins‚ only the L-isomer is found. Serine differs from alanine in that one of the methylenic
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Figure 6: Imatinib The first imatinib drug synthesis was done by Zimmermann (figure 7) in 1993‚ he used a chain of the reaction to reach to imatinib but the important part is that both guanidinium nitrate 7 and aminopyrimidine 8 are precipitated from the respective reaction mixtures by the addition of Figure 7: imatinib synthesis by Zimmermann insolubilizing solvents‚ so we got a condensation reaction between guanidinium salt 7 with enone “9” to form the aminopyrimidine “8” then “8” is
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Hg22+nitrates& nitriles/Hg(NO3)2 in conc. HNO3‚ w/ trace of HNO2/HgSO4‚H2SO4 ‚NaNO2) Hopkins-Cole Test Glyoxylic acid (Mg powder‚ oxalic acid‚ HOAc)‚ conc. H2SO4 Millon’s Test Sakaguchi Test Fohl’s Test Nitroprusside Test Test for Amide Pauly’s Test Alpha-naphthol‚ NaOBr‚ NaOH‚ urea(to stabilize color & destroy excess OBr ions) Pb(CH3COO)2 NaOH Na2Fe(CN)3 in dil. NH3 NaOH Diazo rgt. (1% sulfosalicylic acid with 5% NaNO2)‚ 10% Na2CO3 Reaction/Principle Complexation
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hydrogen chloride. In fact‚ if handled in open air it gives off white smoke owing to the hydrolysis from the moisture in the air. The "smoke" is actually small droplets of hydrochloric acid formed by hydrolysis. http://www.chemguide.co.uk/organicprops/amides/background.html Hydrolysis Acetic anhydride dissolves in water to approximately 2.6% by weight.[10] Aqueous solutions have limited stability because‚ like most acid anhydrides‚ acetic anhydride hydrolyses to give acetic acid:[11] (CH3CO)2O
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Chemistry 116: General Chemistry Syracuse University Project Advance Spring 2009 Exam #4 Name Date 1. The bombardment of with nuclei gives two products‚ one of which is The other product is ________. A. B. C. D. E. 2. The decay of to occurs through the emission of a(n) ________. A. alpha particle B. beta particle C. neutron D. proton E. positron 3. Radionuclides which have too low of a neutron/proton ratio generally decay through ________
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Alanine (ala‚ A) (neutral‚ non-polar) Arginine (arg‚ R) (basic‚ polar) Asparagine (asn‚ N) (neutral‚ polar) Aspartic Acid (asp‚ D) (acidic‚ polar) Cysteine (cys‚ C) (neutral‚ slightly polar) Glutamic Acid (glu‚ E) (acidic‚ polar) Glutamine (gln‚ Q) (neutral‚ polar) Glycine (gly‚ G) (neutral‚ non-polar) Histidine (his‚ H) (basic‚ polar) Isoleucine (ile‚ I) (neutral‚ non-polar) Leucine (leu‚ L) (neutral‚ non-polar) Lysine (lys‚ K) (basic‚ polar) Methionine (met‚
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Experiment 1 Synthesis of Acetaminophen Clifford Tse 20529845 Partner – Raminder Dhanoa TA – Xiao Qi CHEM 123L - 012 February 6‚ 2014 Introduction Acetaminophen‚ also commonly known as Tylenol‚ is an over-the-counter medicine used to relieve pain and reduce fevers. Within this experiment‚ Acetaminophen will be formed through the reaction between p-aminophenol and acetic anhydride. This reaction will incur Acetaminophen as a crude solid being impure‚ which will be purified further through
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RESULTS: Solution | pH Value | Aniline | 7 | Benzyl aniline | 12 | Diethylamine | 10 | Table 1: Basicity of Amines Solution | Odor of Solution | Aniline added with chloroform and alcoholic KOH | Unpleasant smell | Table 2: Carbylamine Test (odor of solution) Solution | Observations | Aniline added with concentrated H2SO4 | -Salt formation upon addition of sulfuric acid- Gelatinous‚ pale yellow solution | Table 3: Salt Formation Solution: | Residue Formation: | pH level:
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(which has no protein present) from the original absorbance the absorbance of the protein at each concentration will remain. Question 7: The Lowry method relies on two different reactions. The first is the formation of a copper ion complex with amide bonds‚ forming reduced copper in alkaline solutions. This is called a "Biuret" chromophore. The second is the reduction of Folin-Ciocalteu reagent (phosphomolybdate and phosphotungstate) by tyrosine and tryptophan residues. The reduced Folin-Ciocalteu
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Bonding Esters contain a carbonyl centre‚ which gives rise to 120°C-C-O and O-C-O angles. Unlike amides‚ esters are structurally flexible functional groups because rotation about the C-O-C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. The pKa of the alpha-hydrogen on esters is around 25. Physical properties and characterization
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