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(10 poinis) What acyclic compound is formed when 6-hexanolactam is reacted with concentrated aqueous HC Hin...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyri...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
Extraction Q1. Why doesn’t the neutral organic compound dissolve in the 1.5 M NaOH solution? Q2....
Extraction Q1. Why doesn’t the neutral organic compound dissolve in the 1.5 M NaOH solution? Q2. Why is diethyl ether a good choice for the organic solvent in this extraction experiment? Q3. What experimental difficulty would you encounter if you neglected to include the drying step before evaporating the ether solution of the neutral organic compound? Q4. Why are the two organic compounds recrystallized before their melting points are determined? Q5. What IR bands are most useful in distinguishing a...
61. What product is finally formed when the initial compound formed from cyclohexanone and pyrrolidine is...
61. What product is finally formed when the initial compound formed from cyclohexanone and pyrrolidine is mixed with allyl chloride and that product is heated and then hydrolyzed? HO ora III A) I B) II C) III D) IV E) V 59. Which reagent would best serve as the basis for a simple chemical test to distinguish between CH3 ? CH3 and M A) NaOI (12 in NaOH) B) Bry/CCL C) CrO3/H2SO4 D) NaHCO3/H20 E) Ag(NH3)2+ 60. What would be...
1. what is the purpose of the following in this experiment: a. concentrated (and not dilute)...
1. what is the purpose of the following in this
experiment:
a. concentrated (and not dilute) hydrochloric acid
b. collecting the distillate in ice
c. sodium bicarbonate extraction
d. water extraction
e. anhydrous sodium or magnesium sulfate
chapter Alkyl Halides and Nucleophilic Aliphatic Substitution 13.1 SYNTHESIS OF BUTYL CHLORIDE Alkyl halides can be prepared by reacting an alcohol with concentrated hydrogen halides: R-OH + H-X- R-OH, R-X. HO where X-CI, Br, I. The reaction of hydrochloric acid with 2 and...
JUL 10 1 и Which of the following is the main product when one mole of...
JUL 10 1 и Which of the following is the main product when one mole of propanone and two moles of benzaldehyde react in the presence of catalytic NaOH and heat? ноо Phcн-сн,с-сн, PhCH=CH-C-CH, "ноо он PHCH-CH2-C-CH2-CHPA PhCH=CH-C-CH=CHPh OAA s Identify the product obtained in the hydrolysis of the following cyclic acid anhydride. CH3 O NO H2O, HCI (complete hydrolysis) A) HO O H + CHÚNHẠC i i . - calu& @ CHỊNH 1 . + CH3NHECI C) Type here...
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with...
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
Construct a flow chart describing the seperation of the mixture and the isolation of each compound...
Construct a flow chart describing the seperation of the
mixture and the isolation of each compound in this experiment. (Lab
steps/procedures includes for reference)
4. Construct a flow chart describing the separation of the mixture and the isolation of each compound in this experiment. A commonly used method of separating a mixture of organic compounds is known as liquid-liquid extraction. Most reactions of organic compounds require extraction at some stage of product purification. In this experiment you will use extraction...
What is the general class of each test reaction in the introduction? Precipitation? Acid-Base? Oxidation eduction?...
What is the general class of each test reaction in the introduction? Precipitation? Acid-Base? Oxidation eduction? anoina to aizy ona svidstils Reaction Class 1 2 iliw 15 TO15192do art sshommua bns nosgol rond dass 101 12575 gbubnium oY noi de lo enor Som 10 910 w II woy Xd on abian aningstid on naloga uzib 3 OOH 4 5 DHET 6 7 SET adus 00 9 Complex ion formation 10 11 No reaction 12 13 14 Combination 15 16 17...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the experimental section above) H2SO4 + Na2Cr207 2H20- H2O, A Molecular Weight Theoretical yield amount moles on (if applicable) Equivalents 2. Look up the melting point for p-nitrobenzoic acid and record the reference. 3. What color change is expected to be observed in the reaction? Explain why. CHROMIC ACID OXIDATION Experimental Procedure: Part I: Synthesis of p-nitrobenzoic Acid 1. Under the hood, add 0.400 g...
18. Which of the following compound(s) would undergo mutarotation in aqueous solution? 19. Draw the chair...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
61. What product is finally formed when the initial compound formed from cyclohexanone and pyrrolidine is mixed with allyl chloride and that product is heated and then hydrolyzed? HO ora III A) I B) II C) III D) IV E) V 59. Which reagent would best serve as the basis for a simple chemical test to distinguish between CH3 ? CH3 and M A) NaOI (12 in NaOH) B) Bry/CCL C) CrO3/H2SO4 D) NaHCO3/H20 E) Ag(NH3)2+ 60. What would be...
1. what is the purpose of the following in this
experiment:
a. concentrated (and not dilute) hydrochloric acid
b. collecting the distillate in ice
c. sodium bicarbonate extraction
d. water extraction
e. anhydrous sodium or magnesium sulfate
chapter Alkyl Halides and Nucleophilic Aliphatic Substitution 13.1 SYNTHESIS OF BUTYL CHLORIDE Alkyl halides can be prepared by reacting an alcohol with concentrated hydrogen halides: R-OH + H-X- R-OH, R-X. HO where X-CI, Br, I. The reaction of hydrochloric acid with 2 and...
JUL 10 1 и Which of the following is the main product when one mole of propanone and two moles of benzaldehyde react in the presence of catalytic NaOH and heat? ноо Phcн-сн,с-сн, PhCH=CH-C-CH, "ноо он PHCH-CH2-C-CH2-CHPA PhCH=CH-C-CH=CHPh OAA s Identify the product obtained in the hydrolysis of the following cyclic acid anhydride. CH3 O NO H2O, HCI (complete hydrolysis) A) HO O H + CHÚNHẠC i i . - calu& @ CHỊNH 1 . + CH3NHECI C) Type here...
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
Construct a flow chart describing the seperation of the
mixture and the isolation of each compound in this experiment. (Lab
steps/procedures includes for reference)
4. Construct a flow chart describing the separation of the mixture and the isolation of each compound in this experiment. A commonly used method of separating a mixture of organic compounds is known as liquid-liquid extraction. Most reactions of organic compounds require extraction at some stage of product purification. In this experiment you will use extraction...
What is the general class of each test reaction in the introduction? Precipitation? Acid-Base? Oxidation eduction? anoina to aizy ona svidstils Reaction Class 1 2 iliw 15 TO15192do art sshommua bns nosgol rond dass 101 12575 gbubnium oY noi de lo enor Som 10 910 w II woy Xd on abian aningstid on naloga uzib 3 OOH 4 5 DHET 6 7 SET adus 00 9 Complex ion formation 10 11 No reaction 12 13 14 Combination 15 16 17...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the experimental section above) H2SO4 + Na2Cr207 2H20- H2O, A Molecular Weight Theoretical yield amount moles on (if applicable) Equivalents 2. Look up the melting point for p-nitrobenzoic acid and record the reference. 3. What color change is expected to be observed in the reaction? Explain why. CHROMIC ACID OXIDATION Experimental Procedure: Part I: Synthesis of p-nitrobenzoic Acid 1. Under the hood, add 0.400 g...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
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