To draw and name all possible aromatic compounds with the molecular formula C 7 H 7 Cl. Concept introduction: All aromatic compounds are derivatives of benzene. The benzene ring accounts for six carbon atoms. The remaining carbons can be attached as alkyl group like methyl, ethyl etc. to the benzene ring. Halogens, if present, can be attached to the benzene ring or to a side chain in the molecule. Monosubstituted benzenes are named by adding the name of the substituent to the parent name benzene. Alkyl-substituted benzenes, called arenes, are named in different ways depending on the size of the alkyl group. If the alkyl group is smaller than the ring (six or fewer carbons), the arene is named as an alkyl-substituted benzene. If the alkyl substituent is larger than the ring (seven or more carbons), the arene is named as a phenyl-substituted alkane . Disubstitutedbenzenes can exist as three isomers such as ortho, meta and para. They are named using the prefixes ortho (o), meta(m) and para (p). An ortho-disubstituted benzene has its two substituent groups in a 1,2-relationship on the ring. A meta-disubstituted benzene has its two substituent groups in a 1,3-relationship on the ring. A para-disubstituted benzene has its two substituent groups in a 1,4-relationship on the ring. While writing the name the substituent groups are arranged alphabetically. To draw and name: All possible aromatic compounds with the molecular formula C 7 H 7 Cl.

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achieve.macmillanlearning.com Canvas EA eac h Hulu YouTube G 3 methyl cyclobutanol - Google Search Ranking Phenol Acidity Course -236 - Organic Chemistry - Mac... ← Assessment Completed 10 of 22 Questions 1 + Netflix paramount plus chem hw Galdehyde reaction with grignard reagent... b My Questions | bartleby M Inbox - chenteislegit@gmail.com - Gmail Due: Fri, Jan 31 Resources Solution Penalized ? Hint Submit Answer Use retrosynthetic analysis to suggest two paths to synthesize 2-methyl-3-hexanol using the Grignard reaction. (Click and drag the appropriate image to the correct position in the reactions.) Route 1 Aldehyde 1 or +98 Aldehyde 2 Route 2 Q6 +100 Solved in 1 attempt Q7 +95 Solved in 2 attempts Q8 +98 Unlimited attempts possible + + Grignard 1 OH H3O+ Grignard 2 Answer Bank Q9 +90 MgBr Unlimited attempts possible CH3CH2CH2MgBr Q10 Unlimited attempts Q11 ? ? +100 in 1 attempt 2-methyl-3-hexanol CH3CH2MgBr H H о H Attempt 3

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Question

Chapter 15.SE, Problem 21AP

Interpretation Introduction

Interpretation:

To draw and name all possible aromatic compounds with the molecular formula C₇H₇Cl.

Concept introduction:

All aromatic compounds are derivatives of benzene. The benzene ring accounts for six carbon atoms. The remaining carbons can be attached as alkyl group like methyl, ethyl etc. to the benzene ring. Halogens, if present, can be attached to the benzene ring or to a side chain in the molecule.

Monosubstituted benzenes are named by adding the name of the substituent to the parent name benzene. Alkyl-substituted benzenes, called arenes, are named in different ways depending on the size of the alkyl group. If the alkyl group is smaller than the ring (six or fewer carbons), the arene is named as an alkyl-substituted benzene. If the alkyl substituent is larger than the ring (seven or more carbons), the arene is named as a phenyl-substituted alkane.

Disubstitutedbenzenes can exist as three isomers such as ortho, meta and para. They are named using the prefixes ortho (o), meta(m) and para (p). An ortho-disubstituted benzene has its two substituent groups in a 1,2-relationship on the ring. A meta-disubstituted benzene has its two substituent groups in a 1,3-relationship on the ring. A para-disubstituted benzene has its two substituent groups in a 1,4-relationship on the ring. While writing the name the substituent groups are arranged alphabetically.

To draw and name:

All possible aromatic compounds with the molecular formula C₇H₇Cl.

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achieve.macmillanlearning.com Canvas EA eac h Hulu YouTube G 3 methyl cyclobutanol - Google Search Ranking Phenol Acidity Course -236 - Organic Chemistry - Mac... ← Assessment Completed 10 of 22 Questions 1 + Netflix paramount plus chem hw Galdehyde reaction with grignard reagent... b My Questions | bartleby M Inbox - chenteislegit@gmail.com - Gmail Due: Fri, Jan 31 Resources Solution Penalized ? Hint Submit Answer Use retrosynthetic analysis to suggest two paths to synthesize 2-methyl-3-hexanol using the Grignard reaction. (Click and drag the appropriate image to the correct position in the reactions.) Route 1 Aldehyde 1 or +98 Aldehyde 2 Route 2 Q6 +100 Solved in 1 attempt Q7 +95 Solved in 2 attempts Q8 +98 Unlimited attempts possible + + Grignard 1 OH H3O+ Grignard 2 Answer Bank Q9 +90 MgBr Unlimited attempts possible CH3CH2CH2MgBr Q10 Unlimited attempts Q11 ? ? +100 in 1 attempt 2-methyl-3-hexanol CH3CH2MgBr H H о H Attempt 3

2) (4 pt) After the reaction was completed, the student collected the following data. Crude product data is the data collected after the reaction is finished, but before the product is purified. "Pure" product data is the data collected after attempted purification using recrystallization. Student B's data: Crude product data "Pure" product data after recrystallization Crude mass: 0.93 g grey solid Crude mp: 96-106 °C Crude % yield: Pure mass: 0.39 g white solid Pure mp: 111-113 °C Pure % yield: a) Calculate the crude and pure percent yields for the student's reaction. b) Summarize what is indicated by the crude and pure melting points.

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