(a)
Interpretation:
The structure for the molecule corresponding to the given IUPAC name, is to be drawn.
Concept introduction:
In the given IUPAC name, the end part of the name indicates the longest continuous carbon chain or largest ring that is established as the root. The suffix ‘ol’ refers to the alcohol
(b)
Interpretation:
The structure for the molecule is to be drawn that corresponds to the given IUPAC name.
Concept introduction:
In the given IUPAC name, the end part of the name indicates the longest continuous carbon chain or largest ring that is established as the root. The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the amine functional group. The locator numbers which are written immediately before the name of substituents indicate the carbon atoms of the root to which they are attached.
(c)
Interpretation:
The structure for the molecule corresponding to the given IUPAC name is to be drawn.
Concept introduction:
In the given IUPAC name, the end part of the name indicates the longest continuous carbon chain or largest ring that is established as the root. The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the amine functional group. The locator numbers which are written immediately before the name of substituents indicate the carbon atoms of the root to which they are attached.
(d)
Interpretation:
The structure for the molecule corresponding to the given IUPAC name is to be drawn.
Concept introduction:
In the given IUPAC name, the end part of the name indicates the longest continuous carbon chain or largest ring that is established as the root. The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the amine functional group. The locator numbers which are written immediately before the name of substituents indicate the carbon atoms of the root to which they are attached.
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Chapter E Solutions
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
- Give their IUPAC names to explain.arrow_forwardOH Amide H-C-0 H 100 (C) (a)arrow_forwardThe correct IUPAC name of the compound Br Ho CH-C- CH но- -CH=CH2 NH2 OH CH 2-amino-3-bromo-4-formyl-3-hydroxy-5-oxohept-6-enoic acid 0 2-amino-3-bromo-4-formyl-3-hydroxy-5-oxohept-6-eneoic acid 6-amino-5-bromo-4-formyl-5-hydroxy-3-oxohept-1-enoic acid 1-amino-2-bromo-2-hydroxy-4-oxo-5-hexen-3-al-1-oic acid 0 2-amino-3-bromo-4-formyl-3-hydroxy-5-oxo-1-heptene carboxylic acidarrow_forward
- Compounds that contain an N-H group associate by hydrogen bonding. (a) Do you expect this association to be stronger or weaker than that of compounds containing an O-H group? (b) Based on your answer to part (a), which would you predict to have the higher boiling point, 1-butanol or 1-butanamine?arrow_forwardCan you draw this with line structure? (a) trimethylamine (b) 1,4-hexanediamine (c) N,N-dibutylamine (d) 2-Methyl-N-propyl-4-octanaminearrow_forwardDraw structures corresponding to these names:(a) 4-Methylpentanamide (b) N-Ethyl-N-methylpropanamidearrow_forward
- Draw structures corresponding to the following names:(a) 2,2,3-Trifluorobutanoic acid(b) 3-Hydroxybutanoic acid(c) 3,3-Dimethyl-4-phenylpentanoic acidarrow_forwardGive suggestion the structural formula for the following compounds. a) m-aminobenzoic acidb) 4-benzyl-2,7-dimethyl-8-phenyloctenearrow_forward2. The functional group given below is characteristic of organic R-C-R (a) ketones (b) acids (c) aldehydes (d) esters (e) alcoholsarrow_forward
- Draw the structural formula for each of the following compounds. a) 2-amino-2,3,4-trimethyl-4-heptene Structure: b) 5-tertbutylnonane Structure: c) 3-hydroxy-2,4,6-trinitrophenol Structure: d) N-ethyl-N-methyl-3-hexanamine Structure: e) 3-oxoheptanal Structure: f) cis-1,2-dimethylcyclopentene Structure:arrow_forwardWhat is the product formed when pentyne reacts with disiamylborane? (A) Pentanol (B) Pentanone (C) Pentanal (D) Pentan-2-olarrow_forwardSphingomyelins, a group of lipids that resemble the membrane phospholipids discussed in Section 3.7, are a major component of the myelin sheath, the insulating layer that surrounds a nerve fiber. (A) What functional groups are present in sphingomyelin X? (B) Classify any alcohol, amine, and amide as 1, 2, or 3. (C) Label the polar head and non polar tails of X.arrow_forward
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