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QUESTION 1 Identify the functional group in the molecule below (there is only one). Spelling counts!...
Identify each functional group shown in bold letters. For each molecule shown below: 1) circle any...
Identify each functional group shown in bold letters. For each molecule shown below: 1) circle any bonds which have considerable polarity, 2) Indicate which atoms arc positive or negative, and 3) tell whether or not the overall molecule is polar The infrared spectrum of a molecule shows peaks at 3000, 1700, 1400 and 1200 cm^-1 Which of the molecules drawn in Part 3 would produce this spectrum? Explain how you made your choice. List each of these halides as primary,...
Question 3 (1 point) Which functional group is found in this molecule? Alcohol Aldehyde Ketone Carboxylic...
Question 3 (1 point) Which functional group is found in this molecule? Alcohol Aldehyde Ketone Carboxylic Acid Question 4 (1 point) Which functional group is found in this molecule? LCHE HE-CH2-CH-CH3 H.COM Alcohol Aldehyde Ketone Carboxylic Acid Question 5 (1 point) Which functional group is found in this molecule? CH2-CH3 Alcohol Aldehyde Ketone Carboxylic Acid Question 6 (1 point) Which functional group is found in this molecule? CH,CH,CCHCH2CH.CH CH Alcohol Aldehyde Ketone Carboxylic Acid Question 7 (1 point) Which functional...
Testbank, Question 005 Identify the functional group in styrene. O ether O alkene O carboxylic acid...
Testbank, Question 005 Identify the functional group in styrene. O ether O alkene O carboxylic acid O aldehyde O ketone Testbank, Question 022 What is the IUPAC name for the following compound? NO Hşco. .CH
QUESTION 15 Which of the following is EXERGONIC? 6 CO2 + 6H20 - glucose + O2...
QUESTION 15 Which of the following is EXERGONIC? 6 CO2 + 6H20 - glucose + O2 fructose 6-phosphate + ATP – fructose 1,6-bisphosphate + ADP (AG = -3.4 kcal/mol) glucose 6-phosphate + ATP – fructose 6-phosphate + ADP (AG = +0.5 kcal/mol) GDP - Pi GTP + H2O QUESTION 17 Fate(s) of pyruvate is(are) Check all that apply. formation of ethyl alcohol by yeasts formation of glucose by gluconeogenesis in liver cells production of ketone bodies formation of lactate under...
Begin by naming the molecule. What functional group could this alcohol be converted to using only...
Begin by naming the molecule.
What functional group could this alcohol be converted to using
only one step?
How many signals would be seen in the 13C NMR
specturm of the alcohol above?
What splitting patterns would be seen in the 1H NMR
spectrum of the alcohol, assuming that the OH proton behaves like a
CH proton in terms of splitting? (single, double, triplet...)
НО,
1. Match each structure to the functional group a alcohol b. aldehyde c. ketone d. acid...
1. Match each structure to the functional group a alcohol b. aldehyde c. ketone d. acid e. esterf. amine HC CH, OH ii. iii. ОН iv. OH H vi. NH2 vii. 2. For each of the following, write the formula (abbreviated) a. OH b. ОН c. 2. What is stereospecificity? Why is it important? 3. For each molecule below, identify the functional groups. НО а. Сн,он СН,ОН ОНИ ОН b. ОН ОН Н.N. О НО. о с.. ОД d. но...
Options for #2: Blank 1: [five/six/seven/eight/nine/ten/other] Blank 2: [pentane/hexane/heptane/octane/nonane/decane/other] Blank 3: [-alcohol/-ether/-ane/-ol/-other] Blank 4: - left...
Options for #2:
Blank 1: [five/six/seven/eight/nine/ten/other]
Blank 2: [pentane/hexane/heptane/octane/nonane/decane/other]
Blank 3: [-alcohol/-ether/-ane/-ol/-other]
Blank 4:
- left to right
- right to left
- clockwise
- counterclockwise
- symmetrical
Blank 5:
- Yes, there is stereochemistry present and must be in the
name
- No, stereochemistry is not present
- No, stereochemistry is present but cannot be assigned
- No, assignable stereochemistry is present but not required in
the name
Question 1 2 pts only HO What functional groups other than...
1)Identify the molecule below with the highest predicted boiling point. Select one: a. pentane b. butanoic...
1)Identify the molecule below with the highest predicted boiling point. Select one: a. pentane b. butanoic acid c. butanol d. butane 2. What the molecule which could be oxidized in a single step to form a carboxylic acid: Select one: a. pentanal b. pentanoic acid c. pentan-2-one d. pentan-1-ol 3. The functional groups which react in an esterification reaction are: Select one: a. carboxyl and amine b. primary hydroxyl and carbonyl c. carboxyl and primary hydroxyl d. carboxyl and carbonyi
1. Provide a complete retrosynthesis and forward synthesis of the target molecule below from the given...
1. Provide a complete retrosynthesis and forward synthesis of the target molecule below from the given starting materials. All carbons of the target must be from the given starting materials. You may use any reagents you find necessary. You may include more than one step over a reaction arrow, but please no more than 3 steps at a time. Please show the key intermediates in your synthesis for partial credit. (10 bonus points) For full credit, include a retrosynthetic analysis,...
Question 1 Identify all compounds below that CANNOT be made by the electrophilic aromatic substitution reactions...
Question 1 Identify all compounds below that CANNOT be made by the electrophilic aromatic substitution reactions introduced in Sections 18.1-18.6 SOH Question 2. Match each pair of structures with the appropriate term. KEY 1 = Constitutional isomers 2 - Diastereomers 0 000 3 = Different conformations 4 = Resonance structures 5 = Bond-shift isomers Question 3. In this reaction, FeBrz is acting as a and the complex that is formed will react with benzene as a/n :Br: : Br-Br: Br-Br-Fe-Br:...
Identify each functional group shown in bold letters. For each molecule shown below: 1) circle any bonds which have considerable polarity, 2) Indicate which atoms arc positive or negative, and 3) tell whether or not the overall molecule is polar The infrared spectrum of a molecule shows peaks at 3000, 1700, 1400 and 1200 cm^-1 Which of the molecules drawn in Part 3 would produce this spectrum? Explain how you made your choice. List each of these halides as primary,...
Question 3 (1 point) Which functional group is found in this molecule? Alcohol Aldehyde Ketone Carboxylic Acid Question 4 (1 point) Which functional group is found in this molecule? LCHE HE-CH2-CH-CH3 H.COM Alcohol Aldehyde Ketone Carboxylic Acid Question 5 (1 point) Which functional group is found in this molecule? CH2-CH3 Alcohol Aldehyde Ketone Carboxylic Acid Question 6 (1 point) Which functional group is found in this molecule? CH,CH,CCHCH2CH.CH CH Alcohol Aldehyde Ketone Carboxylic Acid Question 7 (1 point) Which functional...
Testbank, Question 005 Identify the functional group in styrene. O ether O alkene O carboxylic acid O aldehyde O ketone Testbank, Question 022 What is the IUPAC name for the following compound? NO Hşco. .CH
QUESTION 15 Which of the following is EXERGONIC? 6 CO2 + 6H20 - glucose + O2 fructose 6-phosphate + ATP – fructose 1,6-bisphosphate + ADP (AG = -3.4 kcal/mol) glucose 6-phosphate + ATP – fructose 6-phosphate + ADP (AG = +0.5 kcal/mol) GDP - Pi GTP + H2O QUESTION 17 Fate(s) of pyruvate is(are) Check all that apply. formation of ethyl alcohol by yeasts formation of glucose by gluconeogenesis in liver cells production of ketone bodies formation of lactate under...
Begin by naming the molecule.
What functional group could this alcohol be converted to using
only one step?
How many signals would be seen in the 13C NMR
specturm of the alcohol above?
What splitting patterns would be seen in the 1H NMR
spectrum of the alcohol, assuming that the OH proton behaves like a
CH proton in terms of splitting? (single, double, triplet...)
НО,
1. Match each structure to the functional group a alcohol b. aldehyde c. ketone d. acid e. esterf. amine HC CH, OH ii. iii. ОН iv. OH H vi. NH2 vii. 2. For each of the following, write the formula (abbreviated) a. OH b. ОН c. 2. What is stereospecificity? Why is it important? 3. For each molecule below, identify the functional groups. НО а. Сн,он СН,ОН ОНИ ОН b. ОН ОН Н.N. О НО. о с.. ОД d. но...
Options for #2:
Blank 1: [five/six/seven/eight/nine/ten/other]
Blank 2: [pentane/hexane/heptane/octane/nonane/decane/other]
Blank 3: [-alcohol/-ether/-ane/-ol/-other]
Blank 4:
- left to right
- right to left
- clockwise
- counterclockwise
- symmetrical
Blank 5:
- Yes, there is stereochemistry present and must be in the
name
- No, stereochemistry is not present
- No, stereochemistry is present but cannot be assigned
- No, assignable stereochemistry is present but not required in
the name
Question 1 2 pts only HO What functional groups other than...
1)Identify the molecule below with the highest predicted boiling point. Select one: a. pentane b. butanoic acid c. butanol d. butane 2. What the molecule which could be oxidized in a single step to form a carboxylic acid: Select one: a. pentanal b. pentanoic acid c. pentan-2-one d. pentan-1-ol 3. The functional groups which react in an esterification reaction are: Select one: a. carboxyl and amine b. primary hydroxyl and carbonyl c. carboxyl and primary hydroxyl d. carboxyl and carbonyi
1. Provide a complete retrosynthesis and forward synthesis of the target molecule below from the given starting materials. All carbons of the target must be from the given starting materials. You may use any reagents you find necessary. You may include more than one step over a reaction arrow, but please no more than 3 steps at a time. Please show the key intermediates in your synthesis for partial credit. (10 bonus points) For full credit, include a retrosynthetic analysis,...
Question 1 Identify all compounds below that CANNOT be made by the electrophilic aromatic substitution reactions introduced in Sections 18.1-18.6 SOH Question 2. Match each pair of structures with the appropriate term. KEY 1 = Constitutional isomers 2 - Diastereomers 0 000 3 = Different conformations 4 = Resonance structures 5 = Bond-shift isomers Question 3. In this reaction, FeBrz is acting as a and the complex that is formed will react with benzene as a/n :Br: : Br-Br: Br-Br-Fe-Br:...
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