
(a)
Interpretation:
The given structure has to be classified as an aldehyde, a ketone or neither.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom.
An aldehyde is a carbonyl compound in which the carbonyl carbon atom is bonded to at least one hydrogen atom directly. The other group attached to the carbonyl carbon atom can be alkyl, cycloalkyl, or aryl group.
A ketone is a carbonyl compound in which the carbonyl carbon atom is bonded to two other carbon atoms directly. The groups attached to the carbonyl carbon atom can be alkyl, cycloalkyl, or aryl group.
(b)
Interpretation:
The given structure has to be classified as an aldehyde, a ketone or neither.
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,
An aldehyde is a carbonyl compound in which the carbonyl carbon atom is bonded to at least one hydrogen atom directly. The other group attached to the carbonyl carbon atom can be alkyl, cycloalkyl, or aryl group.
A ketone is a carbonyl compound in which the carbonyl carbon atom is bonded to two other carbon atoms directly. The groups attached to the carbonyl carbon atom can be alkyl, cycloalkyl, or aryl group.
(c)
Interpretation:
The given structure has to be classified as an aldehyde, a ketone or neither.
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,
An aldehyde is a carbonyl compound in which the carbonyl carbon atom is bonded to at least one hydrogen atom directly. The other group attached to the carbonyl carbon atom can be alkyl, cycloalkyl, or aryl group.
A ketone is a carbonyl compound in which the carbonyl carbon atom is bonded to two other carbon atoms directly. The groups attached to the carbonyl carbon atom can be alkyl, cycloalkyl, or aryl group.
(d)
Interpretation:
The given structure has to be classified as an aldehyde, a ketone or neither.
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,
An aldehyde is a carbonyl compound in which the carbonyl carbon atom is bonded to at least one hydrogen atom directly. The other group attached to the carbonyl carbon atom can be alkyl, cycloalkyl, or aryl group.
A ketone is a carbonyl compound in which the carbonyl carbon atom is bonded to two other carbon atoms directly. The groups attached to the carbonyl carbon atom can be alkyl, cycloalkyl, or aryl group.

Trending nowThis is a popular solution!

Chapter 15 Solutions
GENERAL,ORGANIC,+BIO.CHEM.-MINDTAP
- draw the enolate anion and the carbonyl that would be needed to make this product through an aldol addition reaction.arrow_forwardDraw the Michael Adduct and the final product of the Robinson annulation reaction. Ignore inorganic byproducts.arrow_forwardDraw the Michael adduct and final product of the Robinson annulation reaction. Ignore inorganic byproductsarrow_forward
- Post Lab Questions. 1) Draw the mechanism of your Diels-Alder cycloaddition. 2) Only one isomer of product is formed in the Diels-Alder cycloaddition. Why? 3) Imagine that you used isoprene as diene - in that case you don't have to worry about assigning endo vs exo. Draw the "endo" and "exo" products of the Diels-Alder reaction between isoprene and maleic anhydride, and explain why the distinction is irrelevant here. 4) This does not hold for other dienes. Draw the exo and endo products of the reaction of cyclohexadiene with maleic anhydride. Make sure you label your answers properly as endo or exo. 100 °C Xylenes ??? 5) Calculate the process mass intensity for your specific reaction (make sure to use your actual amounts of reagent).arrow_forwardIndicate the product(s) A, B C and D that are formed in the reaction: H + NH-NH-CH [A+B] [C+D] hydrazonesarrow_forwardHow can you prepare a 6 mL solution of 6% H2O2, if we have a bottle of 30% H2O2?arrow_forward
- How many mL of H2O2 from the 30% bottle must be collected to prepare 6 mL of 6% H2O2.arrow_forwardIndicate the product(s) B and C that are formed in the reaction: HN' OCH HC1 B + mayoritario C minoritario OCH3arrow_forwardIndicate the product(s) that are formed in the reaction: NH-NH, OCH3 -H₂O OCH3arrow_forward
- 21.38 Arrange the molecules in each set in order of increasing acidity (from least acidic to most acidic). OH OH SH NH2 8 NH3 OH (b) OH OH OH (c) & & & CH3 NO2 21.39 Explain the trends in the acidity of phenol and the monofluoro derivatives of phenol. OH OH OH OH PK 10.0 PK 8.81 PK 9.28 PK 9.81arrow_forwardidentify which spectrum is for acetaminophen and which is for phenacetinarrow_forwardThe Concept of Aromaticity 21.15 State the number of 2p orbital electrons in each molecule or ion. (a) (b) (e) (f) (c) (d) (h) (i) DA (k) 21.16 Which of the molecules and ions given in Problem 21.15 are aromatic according to the Hückel criteria? Which, if planar, would be antiaromatic? 21.17 Which of the following structures are considered aromatic according to the Hückel criteria? ---0-0 (a) (b) (c) (d) (e) (h) H -H .8.0- 21.18 Which of the molecules and ions from Problem 21.17 have electrons donated by a heteroatom?arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning




