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- 4. Acidity of the H in the structures- which is the most acidic? Arrange in order of increasing acidity. Note: Please note that I was able to determine how to draw skeleton structures without showing the carbons in the terminal ends. The Hs below are bonded to carbons. The first structure has 4 Carbons; the second has 4 and the third has 3. H. H- А H- В9. Rank the following compounds in order of increasing acidity (least acidic < most acidic) [R is an alkyl group and X is Cl, Br, or I]. a. <<< IV b. IV << | < | c. Ieq eq M M M ereg 2req 2req 2req X 2req J F3 $ 4 R C V [Review Topics] [References] Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. 4x Include all valence lone pairs in your answer. • For structures having different hydrogens of comparable acidity, assume that the reaction occurs at the less-substituted carbon. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. ✓✓99.81 O 0- F4 . % 5 T G B F5 *** ^ 6 Cengage Learning Cengage Technical Support Y ChemDoodle H N F6 & N& 7 U O J F7 + [ ] در M 8 PrtScn K F8 9 Home O 83°F Sunny F9 L ) 0 End F10 P Previous C PgUp F11 9 ? Next Save and Exit 9:38 AM 7/18/2022 PgDn F12 0 Ins D Backb) Rank the following alcohols from the most to the least acidic. (liic. НО. CI I но. I || Н ОН I HO CHO H3C-C-CH3 H-C-н Н CH3 " ОН ОН IV c) Indicate the oxidation state for each of the carbon atoms highlighted in red. v. НО F F H-O-OH H₂C-C-H н-с-он V ОН H3C-"-н H3C-C-CH3 ОН IV VConsider the following compounds OH OH D A NH2 H E F The most basic compound is Choose... + The compound(s) that is (are) 2º alcohol Choose... + The compound(s) that is (are) considered as hydrocarbon Choose... The compound that has the strongest hydrogen-bonding is Choose...In the reaction between vanillin and para-toluidine (imine formation) the product is an imine and... оа. water O b. Carbon monoxide О с. NABH4 O d. Carbon dioxide4. The purine heterocycle occurs commonly in the structure of DNA. a. How is each N atom hybridized? b. In what type of orbital does each lone pair on a N atom reside? c. How manyn electrons does purine contain? d. Why is purine aromatic? :N H. purine batond ai enexerlo 08,H HO HO HO b w bemmot etbubong erit wea OH8 HOH2O zhemala eriT nertw bemot78) Why are primary alcohols more acidic than tertiary alcohols, in general? Because tertiary alcohols have less acidic hydrogens. Because primary alcohols have less electron-donating groups which create more effective charge separation between oxygen and hydrogen atom, making it more acidic. Because primary alcohols are more polar than tertiary alcohols. Because primary alcohols have less electron-donating groups which decrease electron density on oxygen, making it more susceptible for H+ to depart from the structure.Ketones typically have a pka of approximately 20. While this is certainly not a strong acid it is much stronger than a typical alkane sp3-CH. using acetone as an example, explain why ketones are much more acidic than Alkanes.SEE MORE QUESTIONS