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(a)
Interpretation:
Two possible structures of cephalin need to be drawn if phosphodiester is in C2 position will there be chirality has to be discussed.
Concept introduction:
Phosphoglycerides are same as triglycerides but the only difference is that in triglycerides there are three fatty acid residues. But in phosphoglyceride one of the fatty acid residue in triglyceride is replaced by a phosphoester. Hydrolysis of phosphoglycerides yield glycerol, fatty acid, phosphate.
To draw: the two possible structure of cephalins
(b)
Interpretation:
Two possible structures of cephalin need to be drawn if phosphodiester is in C2 position will there be chirality has to be discussed.
Concept Introduction:
Chirality is the ability of the compound to rotate the plane polarized light when it is passed through them. A chiral center is the one when the carbon atom is attached to a four different groups. If the plane polarized light is rotated clockwise then the compound is said to be dextrorotatory and if it is anti-clockwise then the compound is levorotatory. If the carbon is not attached to four different groups means then it is said to be achiral.
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Chapter 26 Solutions
ORGANIC CHEMISTRY, WITH SOL. MAN/ STUDY
- I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."arrow_forwardSolve the spectroarrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- Don't used hand raiting and don't used Ai solutionarrow_forward2. 200 LOD For an unknown compound with a molecular ion of 101 m/z: a. Use the molecular ion to propose at least two molecular formulas. (show your work) b. What is the DU for each of your possible formulas? (show your work) C. Solve the structure and assign each of the following spectra. 8 6 4 2 (ppm) 150 100 50 ō (ppm) 4000 3000 2000 1500 1000 500 HAVENUMBERI-11arrow_forwardComplete the spectroscopy with structurearrow_forward
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