Rank these compounds from lowest oxidation level on the left to highest oxidation level on the right. A >>> m HO HO 0 D III H ။ IV Wnong | > ^| > ||| = || ^\| = | > ||| > || | < |V < || < |||
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- ! ( name the organnic compound with explanation)Did you first add the H2O(l) on the right side of the equaton and then added the 2HO- on the left side and multiplied CIO2 on the left side by 2?A glycerol molecule and three butyric acid molecules are shown. Delete atoms and add bonds as necessary to form a triacylglycerol (triglyceride). Draw only the triacylglycerol product. Rings Select / || H ||| H C 0 H с с H-C Draw | H H 0- H -H -0-H H H -0 H More O O C- || UI H₂ C H₂ с H₂ | UF C H₂ с H₂ UI с H₂ CH₂ CH₂ CH₂ ✪ Erase 2 Q
- Give detailed Solution with explanation needed....don't give Handwritten answeraund= ney, churge Na O NH2 attack Tonic c) CH3CH2CH2CH,Li + NH3 (acid CH 3 CH2 CH2-CHz t WH2 (Conj acud) (base) (ca bu 2. The equilibrium idea means that if the reaction is reversible there will be four species in solution at one time, the acid, the base, the conjugate acid, and the conjugate base. Sometimes this is what is required, but at other times we need to choose bases that will completely deprotonate every molecule of acid, i.e. send the reaction completely to the right. These bases will include CH3CH,CH2CH;Li, NaNH2, and LiN(i-Pr)2. Weaker bases will include NaOH, NAOCH3, KOtBu, and NaOCH2CH3. For each of these bases, give the products formed when they react with H2O, then use pKa values to get an idea of the relative base strengths of these compounds. You will provided 7 separate reactions. 3. In CHEM 3112, we will study reactions based on the deprotonation of ketones such as acetone, (CH3)2C=0, which has a pKa of 19. Given the bases LiN(i-Pr)2 and NaOCH3, decide which one…Give detailed Solution with explanation needed..don't give Handwritten answer