IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system. Concept Introduction: IUPAC nomenclature : • 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. Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes . The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers. E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond. Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

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MISSED THIS? Read Section 19.9 (Pages 878-881); Watch IWE 19.10 Consider the following reaction: CH3OH(g) CO(g) + 2H2(g) (Note that AG,CH3OH(g) = -162.3 kJ/mol and AG,co(g)=-137.2 kJ/mol.) Part A Calculate AG for this reaction at 25 °C under the following conditions: PCH₂OH Pco PH2 0.815 atm = 0.140 atm 0.170 atm Express your answer in kilojoules to three significant figures. Ο ΑΣΦ AG = -150 Submit Previous Answers Request Answer □? kJ × Incorrect; Try Again; 2 attempts remaining Calculate the free energy change under nonstandard conditions (AGrxn) by using the following relationship: AGrxn = AGrxn + RTInQ, AGxn+RTInQ, where AGxn is the standard free energy change, R is the ideal gas constant, T is the temperature in kelvins, a is the reaction quotient. Provide Feedback Next >

Answer 1

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Definition Definition Molecules that have multiple bonds between their carbon atoms. Alkenes are hydrocarbons with a double bond between two adjacent carbon atoms (R 2 C=CR 2 ), whereas alkynes are hydrocarbons with a triple bond between two adjacent carbon atoms R-C=C-R . These two groups are known as unsaturated hydrocarbons. They have fewer hydrogen atoms when compared with alkanes with same number of carbon atoms. The general molecular formula for an unsaturated hydrocarbon can be represented as C n H 2n +2 .

Chapter 5.2, Problem 5.5P

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system.

Concept Introduction:

IUPAC nomenclature:

• 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.

Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes.

The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers.

E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond.

Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system.

Concept Introduction:

IUPAC nomenclature:

• 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.

Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes.

The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers.

E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond.

Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system.

Concept Introduction:

IUPAC nomenclature:

• 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.

Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes.

The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers.

E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond.

Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

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MISSED THIS? Read Section 19.9 (Pages 878-881); Watch IWE 19.10 Consider the following reaction: CH3OH(g) CO(g) + 2H2(g) (Note that AG,CH3OH(g) = -162.3 kJ/mol and AG,co(g)=-137.2 kJ/mol.) Part A Calculate AG for this reaction at 25 °C under the following conditions: PCH₂OH Pco PH2 0.815 atm = 0.140 atm 0.170 atm Express your answer in kilojoules to three significant figures. Ο ΑΣΦ AG = -150 Submit Previous Answers Request Answer □? kJ × Incorrect; Try Again; 2 attempts remaining Calculate the free energy change under nonstandard conditions (AGrxn) by using the following relationship: AGrxn = AGrxn + RTInQ, AGxn+RTInQ, where AGxn is the standard free energy change, R is the ideal gas constant, T is the temperature in kelvins, a is the reaction quotient. Provide Feedback Next >

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Answer 2

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Definition Definition Molecules that have multiple bonds between their carbon atoms. Alkenes are hydrocarbons with a double bond between two adjacent carbon atoms (R 2 C=CR 2 ), whereas alkynes are hydrocarbons with a triple bond between two adjacent carbon atoms R-C=C-R . These two groups are known as unsaturated hydrocarbons. They have fewer hydrogen atoms when compared with alkanes with same number of carbon atoms. The general molecular formula for an unsaturated hydrocarbon can be represented as C n H 2n +2 .

Chapter 5.2, Problem 5.5P

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system.

Concept Introduction:

IUPAC nomenclature:

• 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.

Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes.

The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers.

E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond.

Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system.

Concept Introduction:

IUPAC nomenclature:

• 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.

Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes.

The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers.

E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond.

Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system.

Concept Introduction:

IUPAC nomenclature:

• 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.

Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes.

The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers.

E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond.

Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

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Definition Definition Molecules that have multiple bonds between their carbon atoms. Alkenes are hydrocarbons with a double bond between two adjacent carbon atoms (R 2 C=CR 2 ), whereas alkynes are hydrocarbons with a triple bond between two adjacent carbon atoms R-C=C-R . These two groups are known as unsaturated hydrocarbons. They have fewer hydrogen atoms when compared with alkanes with same number of carbon atoms. The general molecular formula for an unsaturated hydrocarbon can be represented as C n H 2n +2 .

Chapter 5.2, Problem 5.5P

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system.

Concept Introduction:

IUPAC nomenclature:

• 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.

Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes.

The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers.

E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond.

Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system.

Concept Introduction:

IUPAC nomenclature:

• 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.

Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes.

The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers.

E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond.

Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given alkene has to be given and the configuration has to be specified by the E, Z system.

Concept Introduction:

IUPAC nomenclature:

• 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.

Alkene: Unsaturated hydrocarbons having at least one double bond between two carbon atoms are known as alkenes.

The systematic name of alkenes are written by replacing “ane” of alkane with the suffix name “ene”. Numbering of the main chain should be in such away that alkene group must get lowest possible numbers.

E configuration: The geometric isomers are given E configuration if high priority groups are placed on opposite sides of the bond.

Z configuration: The geometric isomers are given Z configuration if high priority groups are placed on same sides of the bond.

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Definition Definition Molecules that have multiple bonds between their carbon atoms. Alkenes are hydrocarbons with a double bond between two adjacent carbon atoms (R 2 C=CR 2 ), whereas alkynes are hydrocarbons with a triple bond between two adjacent carbon atoms R-C=C-R . These two groups are known as unsaturated hydrocarbons. They have fewer hydrogen atoms when compared with alkanes with same number of carbon atoms. The general molecular formula for an unsaturated hydrocarbon can be represented as C n H 2n +2 .

Chapter 5.2, Problem 5.5P

(a)

Interpretation Introduction