(a)
Interpretation:
Aldehyde must contain a carbon‑oxygen single bond or not has to be indicated.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom.
The groups that is attached to the carbonyl carbon atom can be either hydrogen or carbon atom. If the attached atoms are hydrogen and a carbon atom means then the compound is an aldehyde and if they are two carbon atoms means then the compound is a ketone. If the attached atom is a nitrogen atom to the carbonyl carbon atom means it is a amide. If a hydroxyl group is attached to a carbonyl carbon atom, then it is a
(b)
Interpretation:
Ketone must contain a carbon‑oxygen single bond or not has to be indicated.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom. Aldehydes and ketones possess this carbonyl functional group in it. The structural representation of a carbonyl group can be given as shown below,
The groups that is attached to the carbonyl carbon atom can be either hydrogen or carbon atom. If the attached atoms are hydrogen and a carbon atom means then the compound is an aldehyde and if they are two carbon atoms means then the compound is a ketone. If the attached atom is a nitrogen atom to the carbonyl carbon atom means it is a amide. If a hydroxyl group is attached to a carbonyl carbon atom, then it is a carboxylic acid. If one of the bonds in the carbonyl carbon atom is attached to an oxygen atom that is bonded with alkyl, cycloalkyl or aromatic system is known as ester.
(c)
Interpretation:
Ester must contain a carbon‑oxygen single bond or not has to be indicated.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom. Aldehydes and ketones possess this carbonyl functional group in it. The structural representation of a carbonyl group can be given as shown below,
The groups that is attached to the carbonyl carbon atom can be either hydrogen or carbon atom. If the attached atoms are hydrogen and a carbon atom means then the compound is an aldehyde and if they are two carbon atoms means then the compound is a ketone. If the attached atom is a nitrogen atom to the carbonyl carbon atom means it is a amide. If a hydroxyl group is attached to a carbonyl carbon atom, then it is a carboxylic acid. If one of the bonds in the carbonyl carbon atom is attached to an oxygen atom that is bonded with alkyl, cycloalkyl or aromatic system is known as ester.
(d)
Interpretation:
Carboxylic acid must contain a carbon‑oxygen single bond or not has to be indicated.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom. Aldehydes and ketones possess this carbonyl functional group in it. The structural representation of a carbonyl group can be given as shown below,
The groups that is attached to the carbonyl carbon atom can be either hydrogen or carbon atom. If the attached atoms are hydrogen and a carbon atom means then the compound is an aldehyde and if they are two carbon atoms means then the compound is a ketone. If the attached atom is a nitrogen atom to the carbonyl carbon atom means it is a amide. If a hydroxyl group is attached to a carbonyl carbon atom, then it is a carboxylic acid. If one of the bonds in the carbonyl carbon atom is attached to an oxygen atom that is bonded with alkyl, cycloalkyl or aromatic system is known as ester.
Want to see the full answer?
Check out a sample textbook solution
Chapter 15 Solutions
GENERAL,ORGANIC,+BIO.CHEM.-MINDTAP
- What is the IUPAC name of the following compound? CH₂CH₂ H CI H₂CH₂C H CH₂ Selected Answer: O (35,4R)-4 chloro-3-ethylpentane Correctarrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electrons-pushing arrows for the following reaction or mechanistic step(s).arrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. I I I H Select to Add Arrows HCI, CH3CH2OHarrow_forward
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and the follow the arrows to draw the intermediate and product in this reaction or mechanistic step(s).arrow_forwardCurved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the intermediates and product of the following reaction or mechanistic step(s).arrow_forwardCurved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the intermediate and the product in this reaction or mechanistic step(s).arrow_forward
- Look at the following pairs of structures carefully to identify them as representing a) completely different compounds, b) compounds that are structural isomers of each other, c) compounds that are geometric isomers of each other, d) conformers of the same compound (part of structure rotated around a single bond) or e) the same structure.arrow_forwardGiven 10.0 g of NaOH, what volume of a 0.100 M solution of H2SO4 would be required to exactly react all the NaOH?arrow_forward3.50 g of Li are combined with 3.50 g of N2. What is the maximum mass of Li3N that can be produced? 6 Li + N2 ---> 2 Li3Narrow_forward
- 3.50 g of Li are combined with 3.50 g of N2. What is the maximum mass of Li3N that can be produced? 6 Li + N2 ---> 2 Li3Narrow_forwardConcentration Trial1 Concentration of iodide solution (mA) 255.8 Concentration of thiosulfate solution (mM) 47.0 Concentration of hydrogen peroxide solution (mM) 110.1 Temperature of iodide solution ('C) 25.0 Volume of iodide solution (1) used (mL) 10.0 Volume of thiosulfate solution (5:03) used (mL) Volume of DI water used (mL) Volume of hydrogen peroxide solution (H₂O₂) used (mL) 1.0 2.5 7.5 Time (s) 16.9 Dark blue Observations Initial concentration of iodide in reaction (mA) Initial concentration of thiosulfate in reaction (mA) Initial concentration of hydrogen peroxide in reaction (mA) Initial Rate (mA's)arrow_forwardDraw the condensed or line-angle structure for an alkene with the formula C5H10. Note: Avoid selecting cis-/trans- isomers in this exercise. Draw two additional condensed or line-angle structures for alkenes with the formula C5H10. Record the name of the isomers in Data Table 1. Repeat steps for 2 cyclic isomers of C5H10arrow_forward
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning