Identify the degree of saturation in the fatty acids shown as line-angle drawings.

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Q: [References] Use the References to access Important values if needed for this question. a. Use…

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Q: Calculate the hydronium ion concentration in an aqueous solution that has a pH of 10.72

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Q: H ball & stick V Strain energy = H H labels Previous

A: There is no strain between gauch CH3:H  Eclipse H:H = 1kcal/mol

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Q: Bu Br ML. से 1) 1.05 nBuLi 2) A) -78 30 min MeOH B-78 to RT for 1h; MeOH e Bu H what would be the…

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Q: Provide the correct IUPAC name for the compound shown here. 4 CI H

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Q: 11. Balance the following reaction in a basic solution. CrO + HSnO₂ → CrO₂ + HSnO,

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Q: Determine four molecular formulas for a compound with a mass spectrum of 222 224 (M: M+2) in a 3:1…

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Q: Why do we not see uranium and thorium in the core even though they are heavier elements

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Q: THE SLOPE OF THE LINE IN THE FOLLOWING GRAPH IS: -35.0 -35.2 In K = -AHIRT+AS" /R In K-10,749/T-27…

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Q: Which is a correct Newman Projection for the following molecule? H. CI F A CH3 H. H CI CH₂CH3 F B…

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Q: 16. Circle and write the name of all the functional groups in the following structure. 0 H -OH 0…

A: A functional group is a group of atoms in a molecule with distinct chemical properties.

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Q: Label the following as cis, trans, or neither. F CI to th CH3 CI H OCH3 H Blank 1 H₂N. Blank 2 H…

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Q: Select the correct substitutive (IUPAC) name for the compound shown below. O…

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Q: What is the formal charge on each indicated atom in the molecule below? Write a numerical value in…

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Q: 200 +

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Q: (g) the meso compound of the following molecule on a Fisher projection H. O CI O CI H #

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Q: Draw all the isomers of C5H₁0. Clearly show stereochemistry if stereoisomers are possible. Step 1:…

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Q: transformation. OH Major synthesis Mini synthesis Draw a synthetic scheme to perform the following…

A: I have given the answer in the explanation section .Hope you will understand that.

Q: After writing their orbital electronic configuration, find the number of unpaired electrons present…

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Q: R req req 2req Keview Topics] Provide an IUPAC name for the structure shown. gy ball & stick Submit…

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Q: Salicylic Acid with Millon’s reagent – To 2 ml. of salicylic acid solution, add 5 drops of Millon’s…

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Q: to HO From Malonic Acid

A: Malonic acid is an example of active methylene compound.

Q: Which of the following is the best method to carry out the following transformation? O 1. BH3 2.…

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Q: ow many monochloro substitution products are produced when the alkanes below are chlorinated?…

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Q: DELLISE 3433.73 Copyright © 1994 1H 13 Proton NHA 180 160 Carbon 13 NMR 18 951 140 HAVEHUMBERS 120…

A: Find the structure of organic compound using ir and nmr spectra

Q: Which of the following alkenes is the most stable? 0

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Q: Select an appropriate name for each compound. OH 5-chloro-3-ethylhexanoic acid…

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Q: (d) Br tok

A: The above reaction will  most likely to proceed through E2 mechanism where E2 stand for bimolecular…

Q: Given the following reactions at 770 K:   XY2Z(g) ↔ XY2(g) + Z2(g)     K = 0.273 XYZ(g) + Y2(g) ↔…

A: The given chemical equations in equilibrium are; XY2Z(g) ⇌ XY2(g) + Z2(g)     K1 = 0.273    -----(1)…

Micelles and Biological Membrane

Micelles are the type of lipid molecules that organize themselves in spherical shape in aqueous solutions. The production of the micelle is a reply to the amphipathic behavior of fatty acids. It means that they consist of both hydrophobic regions and hydrophilic regions. In micelles, polar head groups (hydrophilic groups) produce an outer layer associated with water whereas nonpolar tails (hydrophobic groups) are organized in the interior.