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(a)
Interpretation:
Aldehyde must contain the element nitrogen 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 element nitrogen 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 bond 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 element nitrogen 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 bond 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:
Amide must contain element nitrogen 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 bond in the carbonyl carbon atom is attached to an oxygen atom that is bonded with alkyl, cycloalkyl or aromatic system is known as ester.
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Chapter 15 Solutions
General, Organic, and Biological Chemistry
- Nonearrow_forwardNonearrow_forwardman Campus Depa (a) Draw the three products (constitutional isomers) obtained when 2-methyl-3-hexene reacts with water and a trace of H2SO4. Hint: one product forms as the result of a 1,2-hydride shift. (1.5 pts) This is the acid-catalyzed alkene hydration reaction.arrow_forward
- (6 pts - 2 pts each part) Although we focused our discussion on hydrogen light emission, all elements have distinctive emission spectra. Sodium (Na) is famous for its spectrum being dominated by two yellow emission lines at 589.0 and 589.6 nm, respectively. These lines result from electrons relaxing to the 3s subshell. a. What is the photon energy (in J) for one of these emission lines? Show your work. b. To what electronic transition in hydrogen is this photon energy closest to? Justify your answer-you shouldn't need to do numerical calculations. c. Consider the 3s subshell energy for Na - use 0 eV as the reference point for n=∞. What is the energy of the subshell that the electron relaxes from? Choose the same emission line that you did for part (a) and show your work.arrow_forwardNonearrow_forward(9 Pts) In one of the two Rare Earth element rows of the periodic table, identify an exception to the general ionization energy (IE) trend. For the two elements involved, answer the following questions. Be sure to cite sources for all physical data that you use. a. (2 pts) Identify the two elements and write their electronic configurations. b. (2 pts) Based on their configurations, propose a reason for the IE trend exception. c. (5 pts) Calculate effective nuclear charges for the last electron in each element and the Allred-Rochow electronegativity values for the two elements. Can any of these values explain the IE trend exception? Explain how (not) - include a description of how IE relates to electronegativity.arrow_forward
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