What product would you expect to be formed in the reaction of phenylalanine with ethanol in the presence of hydrogen chloride? (Do not show the amino acid as a zwitterion, show the answer as a neutral amino acid). not show the amino acid as a zv What product would you expe Ph NH3 CH2CH3 Edit Drawing

give detailed solution with explanation needed

envellum.ecollege.com/course.html?courseld3D16522631&OpenVellumHMAC=85a7baea4e7d7b9e1c025b928e35fe16#10001 I Review Constants | Periodic Table The compounds commonly known as "amino acids" are actually a-aminocarboxylic acids. What carbonyl compounds should be used to synthesize the two amino acids shown here using reductive amination? Part A CH3CH NH2 Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. +) H 120 EXP. . i CONT. L. C

Draw the tetrapeptide below out in full chemical structure by attaching the four amino acidsin order (this is an application of the characteristicorganic reaction Formation of an Amide. You can use any chemical notation orcombination of notations to draw your structure, but all bonds and atoms must be shown. Tyr-Cys-Met-His

A. Amino Acids with Electrically Charged Side Chains Negative Pesitive Aspartie Acid Glutamie Acid (Asp D Lysine Histidine Arginine (Argl ® (Glul O (His H HO Ho HO -NH, -NH, NH, NH, -NH, NH NH H,N- ONH, ONH, C. Special Cases B. Amino Acids with Polar Uncharged Side Chains Proline Asparagine (Aan N Cysteine (Cya) © Glycine (Gly O Threonine Glutamine (Pra) P Serine (Ser 9 Но Họ Ho Ho Ho Но NH, NH, NH NH, NH, NH, -NH, но- SH он NH, NH, D. Amino Acids with Hydrophobic Side Chains Leucine (Leu O Phenylalanine (Phe e Tryptophan (Tp W Tyrosine Methionine Valine Isoleucine Alanine (Ala A IMe M Ho Ho Ho Ho HO NH, -NH, Но -NH, HO NH, NH, NH, NH, NH, NH он If the chromatogram was developed from reverse phase conditions, which of the following amino acids is expected to elute first? serine phenylalanine tryptophan O tyrosine

Show how you could us the acetamidomalonate method to prepare the followig amino acids (a)Leucine (b)Tryptophan

Give a clear explanation handwritten answer of all sub parts

kamote tops juice Clear selection In this reaction below, the conjugate base of ethanoic acid is H3C-C O-H H20 H3C-C H30 Н20 H30+ CH3COO- CH3COOH Benedict's reagent is used as a test for the presence of reducing sugars. Molisch test Benedict's test Barfood'o Tast

Suggest a scheme you will follow to synthesise the dipeptide Ala-Gly

Give the sequence of the following tetrapeptide: