Differences between Cis-fatty acid VS. Trans fatty acids
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- Differences between Cis-fatty acid VS. Trans fatty acids
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- Copy and complete the table.
GIVEN: DRAW THE EXPANDED STRUCTURE NAME THE BONDS
[Molecular Orbitals &Hybrid Orbitals]
IUPAC NAME CHOOSE THE SIMPLEST Unsaturated FATTY ACID
NAME OF THE COMPOUND
Cis-fatty acid Trans-fatty acid
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- Instructions: Differences between Cis-fatty acid VS. Trans fatty acids Use white bond paper and blue ink as your writing materials. Handwritten. Copy and complete the table. Given Expanded Structure Name the bonds (Molecular Orbitals & Hybrid Orbitals) IUPAC name 1. Choose the SIMPLEST UNSATURATED FATTY ACID 2. Name of the compound: Cis-fatty acid Trans-fatty acidfunctional groups in palmitic acid, a saturated fatty acid and oleic acid, an unsaturated fatty acidAmino acid isomerism (name types). Isomerism of the carbon skeleton of amino acids - give a few examples.
- Optical isomerism of amino acids. L and D amino acids. Chiral centers of amino acids. Give examples of amino acids that do not have optical isomers.COLOR TESTS FOR PROTEINS AND SPECIFIC AMINO ACIDS Give the name and structure of at least two examples of each of the following: heterocyclic amino acid aromatic amino acid –OH containing amino acid sulfur containing amino acid basic amino acid Acidic amino acid aliphatic non-polar amino acidnot a possible value for the number of monosaccharide units in an oligosaccharide?
- Draw a peptide that includes Phenylalanine, Cysteine, Tyrosine and Tryptophan. Label them by name and abbreviation. Assume a pH of 7 when drawing the protonation state of ionizable chemical groups. Why do the aforementioned aminoacids absorb U-V light?why the notation Ala-Gly-Val-Ala and Ala-Val-Gly-Ala represent two different molecules rather than the same molecule.Chemical properties of fatty acids. Determination of the titer of higher fatty acids in solution. Autooxidation of unsaturated fatty acids.
- using the expanded structure of Levothyroxine. Determine the molecular geometry of each central atom. Color each central atom based on its molecular geometry and include a key for your colors. For example, color tetrahedral C’s red, trigonal planar C’s , blue, etc.Structure activity relationship of pindololBasic chemical properties of amino acids with aromatic radicals in proteins. Use a few examples.