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- To preview image Click Here Provide the missing major organic products, pay attention to stereochemistry as appropriate. B. C. D. E. Br OH CI 1 CHÍNH 2. LIAH, 3. H₂O* H₂O* 1. Mg/THF 2. CO2 3. H₂O 1. Excess MeMgBr 2. H₂O* 1. SOCI₂ 2. =O OHUsing the HSAB theory, predict the direction of the ff. reactions and explain. a. CdI2 + CaF2 ↔️ CdF2+CaI2 b. NH2- + H20 ↔️ NH3 OH- c. H2Po4- + H2O ↔️ H3PO4 + OH-14. For the reaction shown, select the expected major organic product. (see attached screenshot) A. I B. II C. III D. IV E. V
- Provide the major organic product for the 1. LilH 4 2.нсін, о Provide the major organic product of the following reaction. following reaction. ?. 6. Provide the major organic product for the following reaction. HO Br OH NH - Br 1. LIAIH4 2. HC1, H₂O 7. Provide the major organic product of the following reaction. concentrated KMnO4 refluxWhich is the major isolated organic product of this reaction sequence? C B C₂H₂ C3H₂ 1. NaNH, 2. CHI;Br 3. Lindlar's cat., [₂ 4. mcpba (B) C₂H₂ (D) C3H7¹Provide the major organic product of the following reaction. 1. (CH;CH2),NH. H* Ph 2. Na(CH;CO,);BH
- n ane arther. Charge repulsion: the ethylenediamine and its salts The preferred configuration for ethylenediamine are shown below. As you can see, the preferred conformation in each case depends on the protonation state of the amine groups. NH3 NH2 NH2 H. NH3 H. H. ZHN' H. H. H. H H NH3 Build the molecules and explain how the interplay between charge repulsion and hydrogen bonding explain this behavior. 1... Dw.com/ilrn/takeAssignment/takeCovalentActivity.do?locator=Dassignment-take Open Vellum Course Home [Review Topics] [References] 1. H2SO4 Br H20 HO, NaBr + 2. H3C-O H3C-0-Li d = El Elimination f= SN1 Nucleophilic substitution a = Proton transfer e = E2 Elimination g= Sn2 Nucleophilic substitution b = Lewis acid/base c= Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a g fc 1. 2.2. The two molecules A. and B. are in equilibrium in acidic conditions as is shown below. Draw a full arrow pushing mechanism to show how B. is formed from A. – you may draw protonation steps with a generic acid “H-A," as the proton donor. А. В. ОН Cat. HA HO,
- mheducation.com/ext/map/index.html?_con=con&external_browser=D0&launchUrl=https%253A%252F%252Fcompass2g.illinois.edu%252Fweb wing i Saved Complete the reactions to show the synthesis of the following compound from (CH,),CHCH,CH,Br. Part 1: Br K OC(CH3)3 view structure Part 2 out of 2 Br2 H,O What reagent is needed where the "?" is located?HO CI Br b. Fill in the reactants and reagents necessary to make each compound below. a. HO. abel Madc In U Synthesis. Give the reagents necessary for each step. A152 75 4167 Fisnerbran Iter Paper ualitative Cat. No.: 05 09-801A Porosity: Medium Flow Rate: Slow Dia.: 7.0 cm- Pk. of 100 cir Fisher Scientific19) Halohydrin formation from an alkene involves: a. Temporary induction of the dipole moment of a halogen gas.b. Electrophilic attack of pi electrons from the double bond.c. Formation of bromium anion.d. Formation of base as a final product.e. Attack of water molecule as a weak acid.SEE MORE QUESTIONS