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4. In an attempt to make 1-chloro-1-cyclobutylpentane (D), the following reaction sequence was employed. a. Complete...
Need D,E & G. outline a reaction sequence for synthesis of each of the following compounds fr...
need D,E & G. outline a reaction sequence for synthesis of each
of the following compounds from the indicated starting material
& any other organic or inorganic reagents needed.
Outline a reaction sequence for synthesis of each of the following compounds from the indicated starting material and any other organic or inorganic reagents needed. (a) 0 0 0 он OEt он ,EUA 853 PROBLEMS NH+ (g) O OEt OE
Outline a reaction sequence for synthesis of each of the following...
Alkene reaction and mechanisms practice exercise 1) O₃ 2) (CH3)2S 25) Treatment of cyclopentene with peroxybenzoic...
Alkene reaction and mechanisms practice exercise
1) O₃ 2) (CH3)2S 25) Treatment of cyclopentene with peroxybenzoic acid A) results in oxidative cleavage of the ring to produce an acyclic compound B) yields a meso epoxide C) yields an equimolar mixture of enantiomeric epoxides D) gives the same product as treatment of cyclopentene with Os04 E) none of the above 26) Provide a detailed, step-by-step mechanism for the reaction shown below. но Br2 na + HBT Br 27) Provide a detailed,...
The Wittig Reaction 1. Complete the following reactions by filling in the blanks with the correct...
The Wittig Reaction 1. Complete the following reactions by filling in the blanks with the correct structures. (15 pts) NaOH PPhy COOH The scheme above is the reaction you were supposed to perform today. Answer the following question pertaining to the experiment (page 43-44). (a) The first reaction was run in acetone and the product filtered (we can instead, just remove the acetone on the rotary evaporator). What is the product? (5 pts) (b) The product obtained in part 1...
answer all 1. In each of the following, indicate which S2 reaction will occur faster. Explain...
answer all
1. In each of the following, indicate which S2 reaction will occur faster. Explain your reasoning. a. 1-bromo-2,2-dimethylpropane or 1-bromo-3-methylbutane with Nal in DMSO. b. 1-iodopentane with NaN, in ethanol or NaSCH, in ethanol, c. Reaction of isobutyl iodide with NaBr in acetone or in ethanol. 2. In each of the following, indicate which S, 1 reaction will occur faster. Explain your reasoning. a. Reaction of I-chloro-1-methylcyclohexane or 1-chloro-2-methylcyclohexane in aqueous ethanol. b. Reaction of 2-chloropentane or 3-bromohexane...
1) Predict the major product of the following reaction.
1) Predict the major product of the following reaction. 2) What synthetic goal is achieved by subjecting an alkene to an oxymercuration-demercuration sequence? A) syn-hydroxylation B) Markovnikov addition of H2O wherein skeletal rearrangement is prevented C) anti-Markovnikov addition of H2O wherein skeletal rearrangement is promoted D) Markovnikov addition of H2O wherein skeletal rearrangement is promoted E) anti-Markovnikov addition of H20 wherein skeletal rearrangement is prevented 3) Treatment of 2-methylpropene with which of the following reaction conditions results in an anti-Markovnikov addition product? (circle all that apply) A) dry...
Section 4. Total points 26 1. Give one example of each of the following name reactions....
Section 4. Total points 26 1. Give one example of each of the following name reactions. For each reaction, you MUST INCLUDE: i) IUPAC Name of the reactant ii) IUPAC Name of the product iii) Reagents and reaction conditions (4points X 4 = 16 points) a. H.V.Z reaction b. Crossed aldol reaction between an aldehyde and a ketone 2-Propanone Benzaldehple c. Michael reaction between an a.ß unsaturated aldehyde and a B-diketone. d. Dieckman Condensation to have a cyclic product with...
Just need part 2 and 5. 3rd attempt Part 1 Part 2 Part 3 Part 4...
Just need part 2 and 5.
3rd attempt Part 1 Part 2 Part 3 Part 4 Part 5 Parto e Part 1 Correct. Benzene is the inital starting compound of this synthesis. ® Part 2 Did you work backwards and forwards? Did you write a single molecular formula in this box? What chemical reagent is needed to complete this EAS reaction? Part 3 Correct. Benzene is brominated to form bromobenzene in the first step of the reaction Part 4 Correct....
2. Define the following: a. acid-base reaction b. displacement reaction c. oxidation-reduction reaction d. weak electrolyte...
2. Define the following: a. acid-base reaction b. displacement reaction c. oxidation-reduction reaction d. weak electrolyte 115 A Sequence of Chemical Reactions 3. PPPPPPPPPP Identify the following equations as single or double displacement, redox, acid-base, combination, or decompostion reactions. Some may fit in more than one category. a. Cu(s) + 4HNO, (aq) → Cu(NO),(aq) + 2NO, + 2H,0 Mg(s) + H.SO(aq) - MgSo. (aq) + H (6) CuO(s) + HCl(aq) → Cuci (aq) + H,000 d. Cu(NO),(aq) + 2NaOH(aq ->...
Determine the yield limiting reagent and the theoretical yield for the following multistep synthesis from the reaction of ethyl acetoacetate. Draw the chemical complete chemical reaction and mechanism...
Determine the yield limiting reagent and the theoretical yield for the following multistep synthesis from the reaction of ethyl acetoacetate. Draw the chemical complete chemical reaction and mechanism of Product C (determined to be 4-hydroxy-4 4-diphenylbutan-2-one) to Product E provided the procedure below. Procedure Step 4B [Product C to Product E] Place product [C] (0.5 g) in a 50 mL round bottomed flask, add acetone (15 mL), and concentrated HCl (2.5 mL). Boil under reflux on a water bath for...
What is the correct name for the following compound? d) 5-oxo-3-octenoic acid What is the defining...
What is the correct name for the following compound? d) 5-oxo-3-octenoic acid What is the defining functional group of a carboxylic acid? a) an-H attached to a carbonyl group b) an-H attached to a carbon-carbon triple bond c) an-OH attached to a carbonyl group d) an -OH group attached to a O-C double bond e) an-OH group attached to an aromatic ring To convert a carboxylic acid to an aldehyde a) convert the acid to an acid chloride, then use...
need D,E & G. outline a reaction sequence for synthesis of each
of the following compounds from the indicated starting material
& any other organic or inorganic reagents needed.
Outline a reaction sequence for synthesis of each of the following compounds from the indicated starting material and any other organic or inorganic reagents needed. (a) 0 0 0 он OEt он ,EUA 853 PROBLEMS NH+ (g) O OEt OE
Outline a reaction sequence for synthesis of each of the following...
Alkene reaction and mechanisms practice exercise
1) O₃ 2) (CH3)2S 25) Treatment of cyclopentene with peroxybenzoic acid A) results in oxidative cleavage of the ring to produce an acyclic compound B) yields a meso epoxide C) yields an equimolar mixture of enantiomeric epoxides D) gives the same product as treatment of cyclopentene with Os04 E) none of the above 26) Provide a detailed, step-by-step mechanism for the reaction shown below. но Br2 na + HBT Br 27) Provide a detailed,...
The Wittig Reaction 1. Complete the following reactions by filling in the blanks with the correct structures. (15 pts) NaOH PPhy COOH The scheme above is the reaction you were supposed to perform today. Answer the following question pertaining to the experiment (page 43-44). (a) The first reaction was run in acetone and the product filtered (we can instead, just remove the acetone on the rotary evaporator). What is the product? (5 pts) (b) The product obtained in part 1...
answer all
1. In each of the following, indicate which S2 reaction will occur faster. Explain your reasoning. a. 1-bromo-2,2-dimethylpropane or 1-bromo-3-methylbutane with Nal in DMSO. b. 1-iodopentane with NaN, in ethanol or NaSCH, in ethanol, c. Reaction of isobutyl iodide with NaBr in acetone or in ethanol. 2. In each of the following, indicate which S, 1 reaction will occur faster. Explain your reasoning. a. Reaction of I-chloro-1-methylcyclohexane or 1-chloro-2-methylcyclohexane in aqueous ethanol. b. Reaction of 2-chloropentane or 3-bromohexane...
Section 4. Total points 26 1. Give one example of each of the following name reactions. For each reaction, you MUST INCLUDE: i) IUPAC Name of the reactant ii) IUPAC Name of the product iii) Reagents and reaction conditions (4points X 4 = 16 points) a. H.V.Z reaction b. Crossed aldol reaction between an aldehyde and a ketone 2-Propanone Benzaldehple c. Michael reaction between an a.ß unsaturated aldehyde and a B-diketone. d. Dieckman Condensation to have a cyclic product with...
Just need part 2 and 5.
3rd attempt Part 1 Part 2 Part 3 Part 4 Part 5 Parto e Part 1 Correct. Benzene is the inital starting compound of this synthesis. ® Part 2 Did you work backwards and forwards? Did you write a single molecular formula in this box? What chemical reagent is needed to complete this EAS reaction? Part 3 Correct. Benzene is brominated to form bromobenzene in the first step of the reaction Part 4 Correct....
2. Define the following: a. acid-base reaction b. displacement reaction c. oxidation-reduction reaction d. weak electrolyte 115 A Sequence of Chemical Reactions 3. PPPPPPPPPP Identify the following equations as single or double displacement, redox, acid-base, combination, or decompostion reactions. Some may fit in more than one category. a. Cu(s) + 4HNO, (aq) → Cu(NO),(aq) + 2NO, + 2H,0 Mg(s) + H.SO(aq) - MgSo. (aq) + H (6) CuO(s) + HCl(aq) → Cuci (aq) + H,000 d. Cu(NO),(aq) + 2NaOH(aq ->...
What is the correct name for the following compound? d) 5-oxo-3-octenoic acid What is the defining functional group of a carboxylic acid? a) an-H attached to a carbonyl group b) an-H attached to a carbon-carbon triple bond c) an-OH attached to a carbonyl group d) an -OH group attached to a O-C double bond e) an-OH group attached to an aromatic ring To convert a carboxylic acid to an aldehyde a) convert the acid to an acid chloride, then use...
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