
(a)
Interpretation:
Structural formula of Isobutyl amine has to be determined.
Concept introduction:
In chemistry Structure is the arrangement of
Depending on the number of carbon side chain of the amide, different types of amides can form.
From the name of the compound its structure can be determined.
Primary amines can be named in the IUPAC system in several ways,
For simple amines the suffix – amine is added to the name of the alkyl substituent.
The suffix-amine can be used in place of the final –e in the name of the parent compound.
For a secondary amine an N prefixes the compound giving the shorter carbon chain and its chain prefix name.
For a tertiary amine an N, N prefixes the compound giving the two shorter carbon chains and their side chain prefix names.
(b)
Interpretation:
Structural formula of triphenylamine has to be determined.
Concept introduction:
In chemistry Structure is the arrangement of chemical bonds between atoms in a molecule, specifically which atoms are chemically bonded to what other atoms with what kind of chemical bond.
Amines are the derivatives of ammonia
Depending on the number of carbon side chain of the amide, different types of amides can form.
From the name of the compound its structure can be determined.
Primary amines can be named in the IUPAC system in several ways,
For simple amines the suffix – amine is added to the name of the alkyl substituent.
The suffix-amine can be used in place of the final –e in the name of the parent compound.
For a secondary amine an N prefixes the compound giving the shorter carbon chain and its chain prefix name.
For a tertiary amine an N, N prefixes the compound giving the two shorter carbon chains and their side chain prefix names.
(b)
Interpretation:
Structural formula of diisopropylamine has to be determined.
Concept introduction:
In chemistry Structure is the arrangement of chemical bonds between atoms in a molecule, specifically which atoms are chemically bonded to what other atoms with what kind of chemical bond.
Amines are the derivatives of ammonia
Depending on the number of carbon side chain of the amide, different types of amides can form.
From the name of the compound its structure can be determined.
Primary amines can be named in the IUPAC system in several ways,
For simple amines the suffix – amine is added to the name of the alkyl substituent.
The suffix-amine can be used in place of the final –e in the name of the parent compound.
For a secondary amine an N prefixes the compound giving the shorter carbon chain and its chain prefix name.
For a tertiary amine an N, N prefixes the compound giving the two shorter carbon chains and their side chain prefix names.

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Chapter 23 Solutions
Organic Chemistry
- Understanding the general acid-base properties of amino acids O Proteins Imagine each of the molecules shown below was found in an aqueous solution. Can you tell whether the solution is acidic, basic, or neutral? molecule The solution is... 010 H3N-CH-C-OH CH HO CH3 O acidic O basic neutral O (unknown) H3N HO 0 O acidic O basic neutral ○ (unknown) H3N-CH-C-O CH2 CH3-CH-CH3 O acidic O basic Oneutral ○ (unknown) O= X H2N-CH-C-O CH3 CH CH3 acidic O basic O neutral ○ (unknown) ? 000arrow_forwardImagine each of the molecules shown below was found in an aqueous solution. Can you tell whether the solution is acidic, basic, or neutral? molecule 0=0 H3N-CH-C-o HO CH2 OH The solution is... O acidic O basic O neutral O (unknown) H₂N acidic O basic O neutral ○ (unknown) + H3N O OH O acidic O basic O neutral O (unknown) H2N-CH-C-O CH3 O acidic O basic neutral ○ (unknown) X ? olo HEarrow_forwardRecognizing ampli Draw an a amino acid with a methyl (-CH3) side chain. Explanation Check Click and drag to start drawing a structure. X Carrow_forward
- Write the systematic name of each organic molecule: structure name × HO OH ☐ OH CI CI O CI OH OHarrow_forwardく Check the box under each a amino acid. If there are no a amino acids at all, check the "none of them" box under the table. Note for advanced students: don't assume every amino acid shown must be found in nature. COO H3N-C-H CH2 HO CH3 NH3 O CH3-CH CH2 OH Onone of them Explanation Check + H3N O 0. O OH + NH3 CH2 CH3-CH H2N C-COOH H O HIC + C=O H3N-C-O CH3- - CH CH2 OH Х 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Accesarrow_forwardWrite the systematic name of each organic molecule: structure HO-C-CH2-CH3 O -OH CH3-CH2-CH2-CH2-CH2-C-OH CH3 CH3-CH-CH2-C-OH Explanation Check S namearrow_forward
- theres 2 productsarrow_forwardDraw the major product of this solvolysis reaction. Ignore any inorganic byproducts. + CH3CH2OH Drawing Q Atoms, Bonds and Rings OCH2CH3 || OEt Charges OH 00-> | Undo Reset | Br Remove Done Drag To Pan +arrow_forwardDraw the major product of this SN1 reaction. Ignore any inorganic byproducts. CH3CO2Na CH3CO2H Drawing + Br Q Atoms, Bonds and Rings OAC Charges OH ОАс Na ဂ Br Undo Reset Remove Done Drag To Pan +arrow_forward
- Organic Functional Groups entifying positions labeled with Greek letters in acids and derivatives 1/5 ssible, replace an H atom on the a carbon of the molecule in the drawing area with a ce an H atom on the ẞ carbon with a hydroxyl group substituent. ne of the substituents can't be added for any reason, just don't add it. If neither substi er the drawing area. O H OH Oneither substituent can be added. Check D 1 Accessibility ado na witharrow_forwardDifferentiate between electrophilic and nucleophilic groups. Give examples.arrow_forwardAn aldehyde/ketone plus an alcohol gives a hemiacetal, and an excess of alcohol gives an acetal. The reaction is an equilibrium; in aldehydes, it's shifted to the right and in ketones, to the left. Explain.arrow_forward
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