
Concept explainers
(a)
Interpretation:
The wrong thing with the given name of cycloalkane has to be given using IUPAC rules.
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 wrong thing with the given name of cycloalkane has to be given using IUPAC rules.
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 wrong thing with the given name of cycloalkane has to be given using IUPAC rules.
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 wrong thing with the given name of cycloalkane has to be given using IUPAC rules.
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.

Want to see the full answer?
Check out a sample textbook solution
Chapter 1 Solutions
Organic And Biological Chemistry
- Indicate whether the product formed in the reaction exhibits tautomerism. If so, draw the structure of the tautomers. OC2H5 + CoHs-NH-NH,arrow_forwardExplain how substitutions at the 5-position of barbituric acid increase the compound's lipophilicity.arrow_forwardExplain how substitutions at the 5-position of phenobarbital increase the compound's lipophilicity.arrow_forward
- Name an interesting derivative of barbituric acid, describing its structure.arrow_forwardBriefly describe the synthesis mechanism of barbituric acid from the condensation of urea with a β-diketone.arrow_forwardGiven the hydrazones indicated, draw the structures of the enamines that can be formed. Indicate the most stable enamine (explain). C6H5 C6H5 H C6H5 Harrow_forward
- 4. Propose a Synthesis for the molecule below. You may use any starting materials containing 6 carbons or less (reagents that aren't incorporated into the final molecule such as PhзP do not count towards this total, and the starting material can have whatever non-carbon functional groups you want), and any of the reactions you have learned so far in organic chemistry I, II, and III. Your final answer should show each step separately, with intermediates and conditions clearly drawn.arrow_forwardIndicate the importance of the indole ring. Find a representative example and list 5 structures.arrow_forwardΌΗ 1) V2 CO 3 or Nalt In منهarrow_forward
- 6. The equilibrium constant for the reaction 2 HBr (g) → H2(g) + Br2(g) Can be expressed by the empirical formula 11790 K In K-6.375 + 0.6415 In(T K-¹) - T Use this formula to determine A,H as a function of temperature. Calculate A,-H at 25 °C and at 100 °C.arrow_forward3. Nitrosyl chloride, NOCI, decomposes according to 2 NOCI (g) → 2 NO(g) + Cl2(g) Assuming that we start with no moles of NOCl (g) and no NO(g) or Cl2(g), derive an expression for Kp in terms of the equilibrium value of the extent of reaction, Seq, and the pressure, P. Given that K₂ = 2.00 × 10-4, calculate Seq/ of 29/no when P = 0.080 bar. What is the new value по ƒª/ at equilibrium when P = 0.160 bar? Is this result in accord with Le Châtelier's Principle?arrow_forwardConsider the following chemical equilibrium: 2SO2(g) + O2(g) = 2SO3(g) • Write the equilibrium constant expression for this reaction. Now compare it to the equilibrium constant expression for the related reaction: • . 1 SO2(g) + O2(g) = SO3(g) 2 How do these two equilibrium expressions differ? What important principle about the dependence of equilibrium constants on the stoichiometry of a reaction can you learn from this comparison?arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning




