What reactants can be used to synthesize a high yield of 1-halo-1-methylcyclohexane (halo = fluoro, chloro,...
What reactants can be used to synthesize a high yield of 1-halo-1-methylcyclohexane (halo = fluoro, chloro, bromo, or iodo) in the presence of light?
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What reactants can be used to synthesize a high yield of
1-halo-1-methylcyclohexane (halo = fluoro, chloro,...
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Gi...
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Give IUPAC name for the following structure. 3) For each reaction below, indicate which starting material is the Nucleophile and which is the Electrophile. Show arrows to demonstrate how the transformation occurs. →^_^tts a Porto ~ onde gi 4) Draw a mechanism for the conversion of the shown starting material to the corresponding product. 5) In the transformation below, a starting material is treated with HCl to form...
a. What product(s) are expected in the ethoxide-promoted ß-elimination reaction of 1-chloro-1-methylcyclohexane? Omit ions, salts, and...
a. What product(s) are expected in the ethoxide-promoted ß-elimination reaction of 1-chloro-1-methylcyclohexane? Omit ions, salts, and ethanol from your response. b. What product(s) are expected in the ethoxide-promoted ß-elimination reaction of 2-bromo-2,3-dimethylbutane? Omit ions, salts, and ethanol from your response.
What product(s) are expected in the ethoxide-promoted ?-elimination reaction of 1-chloro-1-methylcyclohexane? Omit ions, salts, and ethanol...
What product(s) are expected in the ethoxide-promoted
?-elimination reaction of 1-chloro-1-methylcyclohexane? Omit ions,
salts, and ethanol from your response.
What product(s) are expected in the ethoxide-promoted beta-elimination reaction of 1-chloro-1-methylcyclohexane? Omit ions, salts, and ethanol from your response.
can you help me calculate the theoretical yield calculations for 2 methoxyphenol and 3-chloro-1,2-propanediol THE laboratory...
can you help me calculate the theoretical yield calculations for
2 methoxyphenol and 3-chloro-1,2-propanediol
THE laboratory The essential reactants guaifenesin synthesis are provided in Table 1. Table 1. Compound 2-methoxyphenol bp (°C) Reactants used amount used mmol 550 L calculate MW 124.14 d (g/mL) 1.13 NaOH (25% soln.) 40 do 1 mL obno ethanol 46.07 18 water 142.04 1.32 Sodium sulfate calculate 110.54 500 L (+)-3-chloro-1,2- propanediol 164
Organic Worksheet How can you explain that trams-1-bromo-2-methylcyclohexane yields the non-Zaitsev elimination product 3-methylcylcohexene on treatment...
Organic Worksheet How can you explain that trams-1-bromo-2-methylcyclohexane yields the non-Zaitsev elimination product 3-methylcylcohexene on treatment with base? 1-chloro-1,2-diphenylethane can undergo E2 elimination to give either cis or trans- 1,2,diphenylethylene. Draw Newman projections of the reactive conformations leading to both possible products, and suggest a reason why the trans alkene is the major product.
1. Using the reaction of 2-chloro-1-methylcyclohexane with hydroxide ion, give the mechanism of Sn1 substitution. &...
1. Using the reaction of 2-chloro-1-methylcyclohexane with hydroxide ion, give the mechanism of Sn1 substitution. Complete the question as in question 1 2. Show how you might synthesise the following compounds given the indicated starting materials and anything else you need. In other words, show the reactions that would lead from starting materials to products. Assume that you can purify the products of each reaction. A synthesis may require more than one reaction (products of one reaction are used as starting materials in the...
What alkene and what reagent(s) can be used to synthesize CH3CH2CH2CH(1)CH3
What alkene and what reagent(s) can be used to synthesize CH3CH2CH2CH(1)CH3
please can u answer all of them? thanks 1. What is the IUPAC name for the...
please can u answer all of them? thanks
1. What is the IUPAC name for the following compound? a. a-Chlorovaleryl chloride b. 2-Chloropentanoyl chloride c. 1-Chloropentanoyl chloride d. 1,2-Dichloropentanal e. 1-Chloro-1-butanecarbonyl chloride 2. Which of the following would be the strongest acid? a. 2,3-dimethylhexanoic acid b. 3,3-diiodopentanoic acid c. 3-iodo-4-bromopentanoic acid d. 3-chloro-4-bromohexanoic acid e. 2-fluoro-4-bromopentanoic acid 3. Which of the following would not serve as a synthesis of benzoic acid? HO 1. Cl, NaOH 2. H30 Na Cr207 H2SO4...
6. A student wanted to synthesize the anesthetic CH3 2-ethoxy-2-methylpropane. He used sodium ethoxide 2-chloro-2-methylpropane for...
6. A student wanted to synthesize the anesthetic CH3 2-ethoxy-2-methylpropane. He used sodium ethoxide 2-chloro-2-methylpropane for his synthesis and ended up with no ether. (NaOCH2CH3) and CH2CH 2-ethoxy-2-methylpropane A. What was the product of his synthesis? (1 point) B. What reagents should he have used? (1 point)
What aryl or vinyl halides can be used to synthesize compounds a-c using the Suzuki reagent...
What aryl or vinyl halides can be used to synthesize compounds a-c using the Suzuki reagent shown below? (3 pts.) 1. C. N Suzuki reagent What Gilman reagent can be used to synthesize compounds a-c using the alkyl halide shown below (3 pts.) 2. C. Br a. b. Alkyl Halide
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Give IUPAC name for the following structure. 3) For each reaction below, indicate which starting material is the Nucleophile and which is the Electrophile. Show arrows to demonstrate how the transformation occurs. →^_^tts a Porto ~ onde gi 4) Draw a mechanism for the conversion of the shown starting material to the corresponding product. 5) In the transformation below, a starting material is treated with HCl to form...
What product(s) are expected in the ethoxide-promoted
?-elimination reaction of 1-chloro-1-methylcyclohexane? Omit ions,
salts, and ethanol from your response.
What product(s) are expected in the ethoxide-promoted beta-elimination reaction of 1-chloro-1-methylcyclohexane? Omit ions, salts, and ethanol from your response.
can you help me calculate the theoretical yield calculations for
2 methoxyphenol and 3-chloro-1,2-propanediol
THE laboratory The essential reactants guaifenesin synthesis are provided in Table 1. Table 1. Compound 2-methoxyphenol bp (°C) Reactants used amount used mmol 550 L calculate MW 124.14 d (g/mL) 1.13 NaOH (25% soln.) 40 do 1 mL obno ethanol 46.07 18 water 142.04 1.32 Sodium sulfate calculate 110.54 500 L (+)-3-chloro-1,2- propanediol 164
Organic Worksheet How can you explain that trams-1-bromo-2-methylcyclohexane yields the non-Zaitsev elimination product 3-methylcylcohexene on treatment with base? 1-chloro-1,2-diphenylethane can undergo E2 elimination to give either cis or trans- 1,2,diphenylethylene. Draw Newman projections of the reactive conformations leading to both possible products, and suggest a reason why the trans alkene is the major product.
What alkene and what reagent(s) can be used to synthesize CH3CH2CH2CH(1)CH3
please can u answer all of them? thanks
1. What is the IUPAC name for the following compound? a. a-Chlorovaleryl chloride b. 2-Chloropentanoyl chloride c. 1-Chloropentanoyl chloride d. 1,2-Dichloropentanal e. 1-Chloro-1-butanecarbonyl chloride 2. Which of the following would be the strongest acid? a. 2,3-dimethylhexanoic acid b. 3,3-diiodopentanoic acid c. 3-iodo-4-bromopentanoic acid d. 3-chloro-4-bromohexanoic acid e. 2-fluoro-4-bromopentanoic acid 3. Which of the following would not serve as a synthesis of benzoic acid? HO 1. Cl, NaOH 2. H30 Na Cr207 H2SO4...
6. A student wanted to synthesize the anesthetic CH3 2-ethoxy-2-methylpropane. He used sodium ethoxide 2-chloro-2-methylpropane for his synthesis and ended up with no ether. (NaOCH2CH3) and CH2CH 2-ethoxy-2-methylpropane A. What was the product of his synthesis? (1 point) B. What reagents should he have used? (1 point)
What aryl or vinyl halides can be used to synthesize compounds a-c using the Suzuki reagent shown below? (3 pts.) 1. C. N Suzuki reagent What Gilman reagent can be used to synthesize compounds a-c using the alkyl halide shown below (3 pts.) 2. C. Br a. b. Alkyl Halide
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