
(a)
Interpretation:
Given
Concept Introduction:
- Longest carbon chain has to be identified that is attached to nitrogen atom.
- Suffix “-e” in name of the parent chain
alkane is replaced by “-amine”. - Numbering of the carbon chain is done from the end that is near the nitrogen atom.
- Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.
- In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.
If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary
Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.
Simplest aromatic amine is aniline. Amino group attached to a benzene ring is known as aniline.
(b)
Interpretation:
Given aromatic amine has to be named as derivative of aniline.
Concept Introduction:
IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.
- Longest carbon chain has to be identified that is attached to nitrogen atom.
- Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.
- Numbering of the carbon chain is done from the end that is near the nitrogen atom.
- Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.
- In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.
If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.
Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.
Simplest aromatic amine is aniline. Amino group attached to a benzene ring is known as aniline.
(c)
Interpretation:
Given aromatic amine has to be named as derivative of aniline.
Concept Introduction:
IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.
- Longest carbon chain has to be identified that is attached to nitrogen atom.
- Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.
- Numbering of the carbon chain is done from the end that is near the nitrogen atom.
- Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.
- In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.
If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.
Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.
Simplest aromatic amine is aniline. Amino group attached to a benzene ring is known as aniline.
(d)
Interpretation:
Given aromatic amine has to be named as derivative of aniline.
Concept Introduction:
IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.
- Longest carbon chain has to be identified that is attached to nitrogen atom.
- Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.
- Numbering of the carbon chain is done from the end that is near the nitrogen atom.
- Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.
- In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.
If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.
Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.
Simplest aromatic amine is aniline. Amino group attached to a benzene ring is known as aniline.

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Organic And Biological Chemistry
- QUESTION: Answer Question 5: 'Calculating standard error of regression' STEP 1 by filling in all the empty green boxes *The values are all provided in the photo attached*arrow_forwardpressure (atm) 3 The pressure on a sample of pure X held at 47. °C and 0.88 atm is increased until the sample condenses. The pressure is then held constant and the temperature is decreased by 82. °C. On the phase diagram below draw a path that shows this set of changes. 0 0 200 temperature (K) 400 аarrow_forwarder your payment details | bar xb Home | bartleby x + aleksogi/x/isl.exe/1o u-lgNskr7j8P3jH-1Qs_pBanHhviTCeeBZbufuBYT0Hz7m7D3ZcW81NC1d8Kzb4srFik1OUFhKMUXzhGpw7k1 O States of Matter Sketching a described thermodynamic change on a phase diagram 0/5 The pressure on a sample of pure X held at 47. °C and 0.88 atm is increased until the sample condenses. The pressure is then held constant and the temperature is decreased by 82. °C. On the phase diagram below draw a path that shows this set of changes. pressure (atm) 1 3- 0- 0 200 Explanation Check temperature (K) 400 X Q Search L G 2025 McGraw Hill LLC. All Rights Reserved Terms of Use Privacy Cearrow_forward
- 5.arrow_forward6.arrow_forward0/5 alekscgi/x/sl.exe/1o_u-IgNglkr7j8P3jH-IQs_pBaHhvlTCeeBZbufuBYTi0Hz7m7D3ZcSLEFovsXaorzoFtUs | AbtAURtkqzol 1HRAS286, O States of Matter Sketching a described thermodynamic change on a phase diagram The pressure on a sample of pure X held at 47. °C and 0.88 atm is increased until the sample condenses. The pressure is then held constant and the temperature is decreased by 82. °C. On the phase diagram below draw a path that shows this set of changes. 3 pressure (atm) + 0- 0 5+ 200 temperature (K) 400 Explanation Check X 0+ F3 F4 F5 F6 F7 S 2025 McGraw Hill LLC All Rights Reserved. Terms of Use Privacy Center Accessibility Q Search LUCR + F8 F9 F10 F11 F12 * % & ( 5 6 7 8 9 Y'S Dele Insert PrtSc + Backsarrow_forward
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