TION 8 Which of the following is the major organic product in the reaction sequence? 1. CH;CH-MGCI die th yl ether H3C-CECH 2. H;0* O HO CH-CH3 CHCH2 HO. HO Type: MC
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- Could you please help me with this question I am very stuck. Give the major organic product of each reaction of methyl pentanoate with the given 6 reagents under the conditions shown. Do not draw any byproducts formed. (see photo) a. Reaction with NaOH,H2O heat; then H+,H2O b. Reaction with (CH3)2CHCH2CH2OH(excess), H+ c. Reaction with (CH3CH2)2NH and heat. d. Reaction with CH3MgI(excess), ether; then H+/H2O e. Reaction with LiAlH4, ether; then H+/H2O f. Reaction with DIBAL (diisobutylaluminum hydride), toluene, low temperature; then H+/H2OI recovered 3 mL of water, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O.select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4
- Which compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaFExplain reason behind your option 1.All the following parameters would affect the rate and kinetics of the reaction exceptA.Solvent mediumB.Reaction temperatureC.Reaction timeD.Geometry and structure of the alkyl halideE.pHEXP VIDEO https://www.youtube.com/watch?v=9Wxxv7kwXlA&list=PLE-217H0ao60Uzpzj-FNP_0ScVp5SZB7j&index=8 1.Pre lab question What are the functional groups in your substrate? -Nitrate -Nitrate and acetate -Amide and ether -Benzene ring b.The stable reaction intermediate in this reaction is Nitronium ion Benzonium ion Carbocation Carbanion c.How would you distinguish between 2-nitrophenacetin and 3-nitrophenacetin? -Color difference -Melting point difference -Difference in Molecular weight -They cannot be differentiated. dAn ether group is -Ortho para activating -Meta activating -Ortho para deactivating -ring activator eThe catalyst in this experiment was -Glacial acetic acid -Nitric acid -Sulfuric acid -Ethanol fThe chemical waste from this experiment should be discarded in the -Sink -Halogenated waste container -non-halogenated waste container -Heavy metal waste container. gWhat is the limiting reagent in this experiment? -Nitric acid -Glacial acetic acid -Phenacetin…
- The most common reducing agent used for the conversion of ester into aldehyde. * a-H2/Ni, Heat b-LiAlH4 c-NaBH4 d-DIBAL-HQUESTION 4Predict the products(s) from the reaction of 1-hexyne with each of the following reagents:a) 1 mole of HBrb) H2O, H2SO4, HgSO4c) 2 moles of Br2d) Excess Cl2e) 2 moles of HCl with H2O2f) 1 mole of HClFor problem 8.17, all of the reactions will be SN2. For each reaction, identify and evaluate each nucleophile (strong? weak? Strong or weak as a base?) Also, evaluate each solvent as polar protic or polar aprotic. I recommend drawing the structure of each solvent. (g) Sodium methanethiolate (NaSCH3) in ethanol
- Propose a short synthesis f or ONE of the following molecules. You can start with acetylene, and alkyl halides from 1-4 carbons in length. You can also use an reagents you wish. a) Hexan-3-one (CH3CH2COCH2CH2CH3)I am working on a practice assignment for my organic II course and am having difficulty with a question that asks to identify the reaction sequence used to synthesize isopropylcyclopentane. I would really appreciate the help!For problem 8.17, all of the reactions will be SN2. For each reaction, identify and evaluate each nucleophile (strong? weak? Strong or weak as a base?) Also, evaluate each solvent as polar protic or polar aprotic. I recommend drawing the structure of each solvent. (d) Sodium cyanide in dimethyl sulfoxide (e) Sodium azide in aqueous ethanol (f) Sodium hydrogen sulfide in ethanol