Part 2. Predict the Organic Products. Predict the major organic product(s) for each of the following reactions. Be sure to show stereochemistry when appropriate. 1) BH3/THF 2) H₂O₂/NaOH/H₂O
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Q: answer. Two unique starting materials HBr H3O* ? Br ? *OCH3 大 ? OH 水 OH
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Q: Consider the following cell reaction: Mn(s) + 2 H+(? M) Mn2+(1.00 M) + H2(g)(1.00 atm) If the cell…
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Q: (b) a OH OH Hemiacetal: Acetal: + CH3CCH3 Draw Your Solution
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A: We have find out the mechanism of SN2 reaction.
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Q: Draw the skeletal (line-bond) structure of (1R,2S)-1-bromo-2-methylcyclohexane
A: The given compound is (1R,2S)-1-bromo-2methylcyclohexane.
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Q: Which ion shown has empty 4d orbitals? O Nb OY+ O Mo²+ OZ³+ O Mo
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Q: % Transmittance 100 50 a) 0 4000 inH₂ NH₂ b) 3000 g 2000 NH₂ d) hemistry Steps 1500 Wavenumber…
A: With the help of IR we can identify presence of functional group in the molecule.
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- 1) Redraw the structure and assign E or Z configuration to each double bond in the molecule. 2) Draw the organic products obtained from the ozonolysis of the compound, using a reductive work-up with zinc/HAc.Show stereo chemistry and possible outcomes and the steps for the reaction.The addition of an alcohol to an acid chloride is an example of alcoholysis (alcohol addition with bond breakage). Consider the alcoholysis reaction below and answer the questions that follow. 1. Show the tetrahedral intermediate that is formed after the nucleophilic addition of the alcohol to the acid chloride. Be sure to include all lone pair electrons and formal charges on your intermediate structure. 2. Show the final product of this alcoholysis reaction that forms after the intermediate you made in Part 1. Do not include inorganic or charged products in your answer. Be sure to include all lone pair electrons and formal charges.
- Using your reaction roadmap as a guide, show reagents and conditions to bring about these conversions, which may require more than one step.CH₂ + Using the reagents below, list in order (by letter, no period) those necessary to prepare 2-butyne from acetylene. Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent. a. Br₂, heat, light b. Na, (-H₂) c. Nal(SN2) d. NH4NO3 e. 1) NaNH2, liq. NH3, 2) CH3Br f. (CH3)3COK, (CH3)3COH, heat g. NaOEt, EtOH, heat Step #1 Step #2 Step #31. In the reactions involving the three isomeric alcohols with the formula C4H9OH, describewhat each of the following tests showed about reactivity of the -OH group and reactions of 1°,2°, and 3° alcohols.• the test with neutral KMnO4• the test with concentrated HCl2. Predict how the fourth alcohol with the formula C4H10O would react if tested with:• 0.01 M KMnO4• concentrated HCl at room temperatureExtend FurtherUse your observations of the solutions formed in the previous experiments and yourunderstanding of alcohols to complete a table like the one shown below. Research the meltingand boiling points to verify your answers.
- Illustrated below is the hydrolysis of a C-C bond (in the first molecule) hydrolyzed by water (2nd molecule). Which pair of open boxes best identifies the location of the (-H) and (-OH) components of water on the products. Choose one from the following: (a) A (b) B (c) C (d) DUsing the wittig reaction, synthesise aldehyde 4 to form cis alkene 2, and trans alkene 3. In your answer, with your choice of R group, describe synthetic routes to each alkene and include reagents and conditionsWrite the structure of the principal organic product formed in the reaction of 1-propanol with each of the following reagents:(a) Sulfuric acid (catalytic amount), heat at 140°C(b) Sulfuric acid (catalytic amount), heat at 200°C(c) Dimethyl sulfoxide (DMSO), oxalyl chloride [(COCl)2], triethylamine [N(CH2CH3)3](d) Pyridinium chlorochromate (PCC) in dichloromethane(e) Potassium dichromate (K2Cr2O7) in aqueous sulfuric acid, heat(f) Sodium amide (NaNH2)
- Phineas and Ferbs, two brothers who enjoy vacations, doing fun things every summer. This summer the brothers and their friends carry out an organic synthesis with an unknown compound (L1) that contains 52% Carbon, 6% Hydrogen and 42% bromine, this compound (L1) is treated with magnesium in ether to obtain L2 , which reacts violently with D2O for 1-methyl cyclohexene with a deuterium atom in the methyl group (L3). The L2 reaction is treated with acetone followed by hydrolysis to give L4. Heating L4 with concentrated sulfuric acid gives L5, which decolors the bromine, obtaining L6. L5 undergoes hydrogenation with excess hydrogen and platinum as a catalyst giving rise to isobutyl cyclohexane. Determine the structures of compounds L1 through L6.NH4Cl is sometimes preferred instead of HCl or H2SO4 for “acid” work-up after Grignard reactions, particularly when the expected and desired product is a tertiary alcohol: why?Chhloropropane + sodium ethoxide in the presence of ethanol will yield what products (SN2 reaction). Show the configuration of the product as well as the structural formula