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Concept explainers
(a)
Interpretation:
The IUPAC name for the given cycloalkane has to be written.
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the root name.
Suffix denotes the presence of
Root word represents the longest continuous carbon skeleton of the organic molecule.
The IUPAC name for cycloalkane can be obtained simply by adding prefix cyclo- before the
(b)
Interpretation:
The IUPAC name for the given cycloalkane has to be written.
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the root name.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.
Root word represents the longest continuous carbon skeleton of the organic molecule.
The IUPAC name for cycloalkane can be obtained simply by adding prefix cyclo- before the alkane name which corresponds to the total number of carbon atoms that are present in the ring. To name a cycloalkane, the first step is to find the longest carbon chain that makes a cyclic ring without any unsaturation. The next step is to identify the substituents that are present in the cyclic ring structure. The numbering has to be given in a way that the substituents get the least numbering.
(c)
Interpretation:
The IUPAC name for the given cycloalkane has to be written.
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the root name.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.
Root word represents the longest continuous carbon skeleton of the organic molecule.
The IUPAC name for cycloalkane can be obtained simply by adding prefix cyclo- before the alkane name which corresponds to the total number of carbon atoms that are present in the ring. To name a cycloalkane, the first step is to find the longest carbon chain that makes a cyclic ring without any unsaturation. The next step is to identify the substituents that are present in the cyclic ring structure. The numbering has to be given in a way that the substituents get the least numbering.
(d)
Interpretation:
The IUPAC name for the given cycloalkane has to be written.
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the root name.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.
Root word represents the longest continuous carbon skeleton of the organic molecule.
The IUPAC name for cycloalkane can be obtained simply by adding prefix cyclo- before the alkane name which corresponds to the total number of carbon atoms that are present in the ring. To name a cycloalkane, the first step is to find the longest carbon chain that makes a cyclic ring without any unsaturation. The next step is to identify the substituents that are present in the cyclic ring structure. The numbering has to be given in a way that the substituents get the least numbering.
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Chapter 12 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- How many different stereoisomer forms exist for a biologically-derived aldose with 6 carbons? a) 2 b) 4 c) 8 d) 16 e) None of the abovearrow_forwardIn observing a Haworth or cyclohexane-chair representation of alpha-d-glucopyranose, the anomeric carbon can de best identified by: a) the carbon atom which is bonded to the most H atoms b) the carbon atom which is bonded to the least H atoms c) The carbon atom which has its OH group pointing down d) The carbon atom which is bonded to two oxygen atoms Cellulose differs from amylose in that: a) cellulose has 1-6 branches while amylose does not b) amylose has 1-6 branches while cellulose does not c) amylose has alpha glycosidic bonds while cellulose has beta glycosidic bonds d) cellulose contains sulfate while amylose does not. The glycosaminoglycan (mucopolysaccharide) which is not normally associated with joint tissue is: a) heparin b) keratan sulfate c) chondroitin sulfate d) hyaluronic acid In glycoproteins, which amino acid does not bond sugar molecules? a) Asn b) Ser c) Thr d) Gly Which feature do all lipid molecules share in common? a) fatty acid molecules…arrow_forwardExamine the structure shown below. A) What is the common name for this fatty acid? B) What is the IUPAC Name for this fatty acid? (Note: you can use the letter D to represent A in the name).arrow_forward
- Consider olive oil, an oil with a high percentage of fat derived from oleic acid (otherwise known as cis[18:1] fatty acid). a, Explain why such a structure may allow olive oil to be one of the "healthier" oils? b, why such a structure may allow olive oil to be a liquid at room temperature, while butter and lard are solid at room temperature? c, why such a structure may cause olive oil to be prone to oxidative damage upon exposure to air and heat?arrow_forwardStearidonic acid (C18H28O2) is an unsaturated fatty acid obtained from oils isolated from hemp and blackcurrant (see also Problem 10.11). a. What fatty acid is formed when stearidonic acid is hydrogenated with excess Hạ and a Pd catalyst? b. What fatty acids are formed when stearidonic acid is hydrogenated with one equivalent of Hz and a Pd catalyst? c. Draw the structure of a possible product formed when stearidonic acid is hydrogenated with one equivalent of H2 and a Pd catalyst, and one double OH stearidonic acid bond is isomerized to a trans isomer. d. How do the melting points of the following fatty acids compare: stearidonic acid; one of the products formed in part (b); the product drawn in part (c)?arrow_forwardResearch the IUPAC and common names and the short-hand codes of the following: 9 saturated fatty acids (4C-20C atoms) 5 unsaturated fatty acids (16C-20C atoms) 3 essential fatty acids 4 eicosanoidsarrow_forward
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