The structure of structural isomer of the isooctane, 2,2,4-trimethylpentane which has molecular formula C 8 H 18 has to be drawn. Another two structural isomers of C 8 H 18 which has longest five carbon chain has to be drawn and thier systematic name has to be written . Concept introduction: Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word. Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc… Suffix represents the substituent present in the molecule. It can be any alkene , alkyne , alcohol, carboxylic acid ... Root word represents the longest continuous carbon skeleton present in the organic molecule. When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo. IUPAC naming for Alkane: Name the main chain: Find the longest carbon chain and name the chain according to the number of carbon atoms it contains; is also the suffix part of the name. Number the carbon atoms in the main chain: The carbons are numbered, in which the substituents must get lowest possible numbers. Identify the substituents, and number each: The number at where substituents are present has to be noted. The substituents written as prefix. Write the names as a single word: Use the hyphen to separate the numbers from the different prefix; commas to separate numbers. If two or more different substituents are present, arrange them in alphabetical order. If two or more identical substituents are present, use prefixes di-, tri-, tetra-, but this particular prefix should not be used for alphabetizing purpose. Isomersim: Compounds having same molecular formula but exhibit different structures called isomers.This phenomenon is known as isomersim Structural Isomers are the possible structures of a molecule with same molecular formula but have different arrangements of bonds and atoms. For a single molecular formula of alkanes higher than propane different arrangements of atoms can give a different structure.

Question

What spectral features allow you to differentiate the product from the starting material? Use four separate paragraphs for each set of comparisons. You should have one paragraph each devoted to MS, HNMR, CNMR and IR. 2) For MS, the differing masses of molecular ions are a popular starting point. Including a unique fragmentation is important, too. 3) For HNMR, CNMR and IR state the peaks that are different and what makes them different (usually the presence or absence of certain groups). See if you can find two differences (in each set of IR, HNMR and CNMR spectra) due to the presence or absence of a functional group. Include peak locations. Alternatively, you can state a shift of a peak due to a change near a given functional group. Including peak locations for shifted peaks, as well as what these peaks are due to. Ideally, your focus should be on not just identifying the differences but explaining them in terms of functional group changes.

Answer 1

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 23, Problem 6PS

Interpretation Introduction

Interpretation: The structure of structural isomer of the isooctane, 2,2,4-trimethylpentane which has molecular formula C8H18 has to be drawn. Another two structural isomers of C8H18 which has longest five carbon chain has to be drawn and thier systematic name has to be written .

Concept introduction:

Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc…

Suffix represents the substituent present in the molecule. It can be any alkene, alkyne, alcohol, carboxylic acid...

Root word represents the longest continuous carbon skeleton present in the organic molecule.

When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo.

IUPAC naming for Alkane:

Name the main chain: Find the longest carbon chain and name the chain according to the number of carbon atoms it contains; is also the suffix part of the name.

Number the carbon atoms in the main chain: The carbons are numbered, in which the substituents must get lowest possible numbers.

Identify the substituents, and number each: The number at where substituents are present has to be noted. The substituents written as prefix.

Write the names as a single word: Use the hyphen to separate the numbers from the different prefix; commas to separate numbers. If two or more different substituents are present, arrange them in alphabetical order. If two or more identical substituents are present, use prefixes di-, tri-, tetra-, but this particular prefix should not be used for alphabetizing purpose.

Isomersim: Compounds having same molecular formula but exhibit different structures called isomers.This phenomenon is known as isomersim

Structural Isomers are the possible structures of a molecule with same molecular formula but have different arrangements of bonds and atoms. For a single molecular formula of alkanes higher than propane different arrangements of atoms can give a different structure.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

What spectral features allow you to differentiate the product from the starting material? Use four separate paragraphs for each set of comparisons. You should have one paragraph each devoted to MS, HNMR, CNMR and IR. 2) For MS, the differing masses of molecular ions are a popular starting point. Including a unique fragmentation is important, too. 3) For HNMR, CNMR and IR state the peaks that are different and what makes them different (usually the presence or absence of certain groups). See if you can find two differences (in each set of IR, HNMR and CNMR spectra) due to the presence or absence of a functional group. Include peak locations. Alternatively, you can state a shift of a peak due to a change near a given functional group. Including peak locations for shifted peaks, as well as what these peaks are due to. Ideally, your focus should be on not just identifying the differences but explaining them in terms of functional group changes.

Question 6 What is the major product of the following Diels-Alder reaction? ? Aldy by day of A. H о B. C. D. E. OB OD Oc OE OA

None

Answer 2

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 23, Problem 6PS

Interpretation Introduction

Interpretation: The structure of structural isomer of the isooctane, 2,2,4-trimethylpentane which has molecular formula C8H18 has to be drawn. Another two structural isomers of C8H18 which has longest five carbon chain has to be drawn and thier systematic name has to be written .

Concept introduction:

Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc…

Suffix represents the substituent present in the molecule. It can be any alkene, alkyne, alcohol, carboxylic acid...

Root word represents the longest continuous carbon skeleton present in the organic molecule.

When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo.

IUPAC naming for Alkane:

Name the main chain: Find the longest carbon chain and name the chain according to the number of carbon atoms it contains; is also the suffix part of the name.

Number the carbon atoms in the main chain: The carbons are numbered, in which the substituents must get lowest possible numbers.

Identify the substituents, and number each: The number at where substituents are present has to be noted. The substituents written as prefix.

Write the names as a single word: Use the hyphen to separate the numbers from the different prefix; commas to separate numbers. If two or more different substituents are present, arrange them in alphabetical order. If two or more identical substituents are present, use prefixes di-, tri-, tetra-, but this particular prefix should not be used for alphabetizing purpose.

Isomersim: Compounds having same molecular formula but exhibit different structures called isomers.This phenomenon is known as isomersim

Structural Isomers are the possible structures of a molecule with same molecular formula but have different arrangements of bonds and atoms. For a single molecular formula of alkanes higher than propane different arrangements of atoms can give a different structure.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 3

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 23, Problem 6PS

Interpretation Introduction

Interpretation: The structure of structural isomer of the isooctane, 2,2,4-trimethylpentane which has molecular formula C8H18 has to be drawn. Another two structural isomers of C8H18 which has longest five carbon chain has to be drawn and thier systematic name has to be written .

Concept introduction:

Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc…

Suffix represents the substituent present in the molecule. It can be any alkene, alkyne, alcohol, carboxylic acid...

Root word represents the longest continuous carbon skeleton present in the organic molecule.

When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo.

IUPAC naming for Alkane:

Name the main chain: Find the longest carbon chain and name the chain according to the number of carbon atoms it contains; is also the suffix part of the name.

Number the carbon atoms in the main chain: The carbons are numbered, in which the substituents must get lowest possible numbers.

Identify the substituents, and number each: The number at where substituents are present has to be noted. The substituents written as prefix.

Write the names as a single word: Use the hyphen to separate the numbers from the different prefix; commas to separate numbers. If two or more different substituents are present, arrange them in alphabetical order. If two or more identical substituents are present, use prefixes di-, tri-, tetra-, but this particular prefix should not be used for alphabetizing purpose.

Isomersim: Compounds having same molecular formula but exhibit different structures called isomers.This phenomenon is known as isomersim

Structural Isomers are the possible structures of a molecule with same molecular formula but have different arrangements of bonds and atoms. For a single molecular formula of alkanes higher than propane different arrangements of atoms can give a different structure.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 4

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 23, Problem 6PS

Interpretation Introduction