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2. Draw structural formulas of the following compounds. Circle and idet are present in each compound....
Instructor approval Read the lab report. Date: 1. Define the following terms in your own words....
Instructor approval Read the lab report. Date: 1. Define the following terms in your own words. a. Chromatography b. analgesic 2. Draw structural formulas of the following compounds. Circle and identify the are present in each compound. mg compounds. Circle and identify the functional groups that a. Aspirin b. Ibuprofen c. Acetaminophen d. Caffeine 11-1
Need help on these questions 1) Draw condensed structural formulas for the following organic compounds Organic...
Need help on these questions
1) Draw condensed structural formulas for the following organic compounds Organic Name Condensed Structural Formula 1,1,1-trichloroethane (2) 2,3-dibromo-1-fluoro-2,4,5- trimethylhexane (4) 2,2-dimethylpropane (2) 2) Draw the line structural formulas for the following organic compounds Organic Name Line Structural Formula 3-isopropylhexane (2) 1,1,2-tribromopropane (2) 2,3,5,5-tetramethyloctane (2) 5) For the following organic molecule put circles around primary carbons squares around secondary carbons, triangles around tertiary carbons.(3) CH3 CHз I CH2-C I -CH— сHз CH2 CH3 I CHз 6)...
a. For each pair of compounds, tell whether the structural formulas shown represent the same compound,...
a. For each pair of compounds, tell whether the structural formulas shown represent the same compound, different compounds that are constitutional isomers or different compounds that are not constitutional isomers. [4 x 1 mark] (1) and (11) and (111) and (iv) and b. Draw a structural formula for each compound. 1 (3E, 62) 2,9-dimethyl-3,6-decadiene (i) 1,6-Heptadiyne (111) 3-phenyl-1.3-butanediol [1 mark] [1 mark] [1 mark] c. Give TWO chemical tests which are indicated by a change in colour, (write the equation...
1. Identify all the functional groups in the following compounds. Circle each functional group and label...
1. Identify all the functional groups in the following
compounds. Circle each functional group and label each group.
Thank you!
1. Identify all the functional groups in the following compounds. Circle each functional group and label each group. Hiç O CH CH CH-C-0-CHCH, -0-CH, CH CH(CH), a. acid group СОН) -CH-CHNHA 0-C-CH Amphetamine (a central nervous system stimulant and abused drug) O Aspirin ( 13 H1802 . . HC=CHCHACHACHCH CHO CHE e. HCCHI (CH OH CHE Citronellal alcohol group ~...
Enol Forms of Carbonyl Compounds Draw structural formulas for all of the enol forms of the...
Enol Forms of Carbonyl Compounds
Draw structural formulas for all of the enol forms of the
carbonyl compound below.
Draw structural formulas for all of the enol forms of the carbonyl compound belon OCH3 You do not have to consider stereochemistry. .Consider stereoisomeric enols as a single enol form. In the case of dicarbonyl compounds, do not include stuctures in which both carbonyl groups are present as enols. Draw one structure per sketcher. Add additional sketchers using the drop-down menu...
Draw the condensed and line-angle structural formulas for each of the following compounds: a. butyraldehyde b....
Draw the condensed and line-angle structural formulas for each of the following compounds: a. butyraldehyde b. 3, 4-dichloropentanal c. 4-bromobutanone d. acetone
Draw structural formulas for all of the enol forms of the carbonyl compound below. • You...
Draw structural formulas for all of the enol forms of the carbonyl compound below. • You do not have to consider stereochemistry. • Consider stereoisomeric enols as a single enol form. . In the case of dicarbonyl compounds, do not include stuctures in which both carbonyl groups are present as enols. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner . Separate structures with + signs from the drop-down menu -O0O-...
QUESTIONS 1. In your own words, explain how the components of a mixture are separated during...
QUESTIONS 1. In your own words, explain how the components of a mixture are separated during thin layer chromatography. Do not explain how to perform TLC; in other words do not explain the procedure. 2. Explain the purpose of the UV lamp in this experiment. 3. Why must you use pencil, not pen, when you make marks on the TLC plate? How do you know? Be sure to 4. Which substances were in the OTC pain reliever? discuss your Rr...
3. Draw the structural formulas for the following compounds. (10 points, 2 each) a. 2-propanol b....
3. Draw the structural formulas for the following compounds. (10 points, 2 each) a. 2-propanol b. 2-methyl-5-hexene-2-ol c. 3-cyclohexenol d. 4-nitrophenol e. phenol 4. Classify the following substituents as ortho/para or meta directing and activating or deactivating (two part answer for each group) (note the line 34 indicates where the group is attached to the benzene ring. (12points, 2 each) NH2 Ooh &r HC-CH₃ No? QH
9. Draw the structural formulas for the following compounds: a. 1-bromobutane b. 2-bromobutane c. 1, 2-dibromobutane...
9. Draw the structural formulas for the following compounds: a. 1-bromobutane b. 2-bromobutane c. 1, 2-dibromobutane d. 1, 3-dibromobutane e. 1, 4-dibromobutane f. 2, 3-dibromobutane
Instructor approval Read the lab report. Date: 1. Define the following terms in your own words. a. Chromatography b. analgesic 2. Draw structural formulas of the following compounds. Circle and identify the are present in each compound. mg compounds. Circle and identify the functional groups that a. Aspirin b. Ibuprofen c. Acetaminophen d. Caffeine 11-1
Need help on these questions
1) Draw condensed structural formulas for the following organic compounds Organic Name Condensed Structural Formula 1,1,1-trichloroethane (2) 2,3-dibromo-1-fluoro-2,4,5- trimethylhexane (4) 2,2-dimethylpropane (2) 2) Draw the line structural formulas for the following organic compounds Organic Name Line Structural Formula 3-isopropylhexane (2) 1,1,2-tribromopropane (2) 2,3,5,5-tetramethyloctane (2) 5) For the following organic molecule put circles around primary carbons squares around secondary carbons, triangles around tertiary carbons.(3) CH3 CHз I CH2-C I -CH— сHз CH2 CH3 I CHз 6)...
a. For each pair of compounds, tell whether the structural formulas shown represent the same compound, different compounds that are constitutional isomers or different compounds that are not constitutional isomers. [4 x 1 mark] (1) and (11) and (111) and (iv) and b. Draw a structural formula for each compound. 1 (3E, 62) 2,9-dimethyl-3,6-decadiene (i) 1,6-Heptadiyne (111) 3-phenyl-1.3-butanediol [1 mark] [1 mark] [1 mark] c. Give TWO chemical tests which are indicated by a change in colour, (write the equation...
1. Identify all the functional groups in the following
compounds. Circle each functional group and label each group.
Thank you!
1. Identify all the functional groups in the following compounds. Circle each functional group and label each group. Hiç O CH CH CH-C-0-CHCH, -0-CH, CH CH(CH), a. acid group СОН) -CH-CHNHA 0-C-CH Amphetamine (a central nervous system stimulant and abused drug) O Aspirin ( 13 H1802 . . HC=CHCHACHACHCH CHO CHE e. HCCHI (CH OH CHE Citronellal alcohol group ~...
Enol Forms of Carbonyl Compounds
Draw structural formulas for all of the enol forms of the
carbonyl compound below.
Draw structural formulas for all of the enol forms of the carbonyl compound belon OCH3 You do not have to consider stereochemistry. .Consider stereoisomeric enols as a single enol form. In the case of dicarbonyl compounds, do not include stuctures in which both carbonyl groups are present as enols. Draw one structure per sketcher. Add additional sketchers using the drop-down menu...
Draw the condensed and line-angle structural formulas for each of the following compounds: a. butyraldehyde b. 3, 4-dichloropentanal c. 4-bromobutanone d. acetone
Draw structural formulas for all of the enol forms of the carbonyl compound below. • You do not have to consider stereochemistry. • Consider stereoisomeric enols as a single enol form. . In the case of dicarbonyl compounds, do not include stuctures in which both carbonyl groups are present as enols. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner . Separate structures with + signs from the drop-down menu -O0O-...
QUESTIONS 1. In your own words, explain how the components of a mixture are separated during thin layer chromatography. Do not explain how to perform TLC; in other words do not explain the procedure. 2. Explain the purpose of the UV lamp in this experiment. 3. Why must you use pencil, not pen, when you make marks on the TLC plate? How do you know? Be sure to 4. Which substances were in the OTC pain reliever? discuss your Rr...
3. Draw the structural formulas for the following compounds. (10 points, 2 each) a. 2-propanol b. 2-methyl-5-hexene-2-ol c. 3-cyclohexenol d. 4-nitrophenol e. phenol 4. Classify the following substituents as ortho/para or meta directing and activating or deactivating (two part answer for each group) (note the line 34 indicates where the group is attached to the benzene ring. (12points, 2 each) NH2 Ooh &r HC-CH₃ No? QH
9. Draw the structural formulas for the following compounds: a. 1-bromobutane b. 2-bromobutane c. 1, 2-dibromobutane d. 1, 3-dibromobutane e. 1, 4-dibromobutane f. 2, 3-dibromobutane
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