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(a)
Interpretation: The IUPAC names of the compounds have to be given.
Concept Introduction:
The IUPAC names of organic compounds are given by
IUPAC naming of Ether compounds:
An Ether group consists of Oxygen atom attached between two Carbon chains. The shorter of two chains becomes the first part of the name with ‘ane’ changes to ‘oxy’ and the longer
When the Oxygen is not attached to the end of main chain of alkane, then the shorter alkyl group and the Ether group is treated as side chain and prefixed with its binding position on the main chain.
(b)
Interpretation: The IUPAC names of the compounds have to be given.
Concept Introduction:
The IUPAC names of organic compounds are given by IUPAC nomenclature of organic chemistry. The standard method of assigning a name to organic chemical compound is done by IUPAC (International Union of Pure and Applied Chemistry).
IUPAC naming of Ether compounds:
An Ether group consists of Oxygen atom attached between two Carbon chains. The shorter of two chains becomes the first part of the name with ‘ane’ changes to ‘oxy’ and the longer alkane becomes the suffix of the name of the ether.
When the Oxygen is not attached to the end of main chain of alkane, then the shorter alkyl group and the Ether group is treated as side chain and prefixed with its binding position on the main chain.
(c)
Interpretation: The IUPAC names of the compounds have to be given.
Concept Introduction:
The IUPAC names of organic compounds are given by IUPAC nomenclature of organic chemistry. The standard method of assigning a name to organic chemical compound is done by IUPAC (International Union of Pure and Applied Chemistry).
IUPAC naming of Ether compounds:
An Ether group consists of Oxygen atom attached between two Carbon chains. The shorter of two chains becomes the first part of the name with ‘ane’ changes to ‘oxy’ and the longer alkane becomes the suffix of the name of the ether.
When the Oxygen is not attached to the end of main chain of alkane, then the shorter alkyl group and the Ether group is treated as side chain and prefixed with its binding position on the main chain.
(d)
Interpretation: The IUPAC names of the compounds have to be given.
Concept Introduction:
The IUPAC names of organic compounds are given by IUPAC nomenclature of organic chemistry. The standard method of assigning a name to organic chemical compound is done by IUPAC (International Union of Pure and Applied Chemistry).
IUPAC naming of Ether compounds:
An Ether group consists of Oxygen atom attached between two Carbon chains. The shorter of two chains becomes the first part of the name with ‘ane’ changes to ‘oxy’ and the longer alkane becomes the suffix of the name of the ether.
When the Oxygen is not attached to the end of main chain of alkane, then the shorter alkyl group and the Ether group is treated as side chain and prefixed with its binding position on the main chain.
(e)
Interpretation: The IUPAC names of the compounds have to be given.
Concept Introduction:
The IUPAC names of organic compounds are given by IUPAC nomenclature of organic chemistry. The standard method of assigning a name to organic chemical compound is done by IUPAC (International Union of Pure and Applied Chemistry).
IUPAC naming of Ether compounds:
An Ether group consists of Oxygen atom attached between two Carbon chains. The shorter of two chains becomes the first part of the name with ‘ane’ changes to ‘oxy’ and the longer alkane becomes the suffix of the name of the ether.
When the Oxygen is not attached to the end of main chain of alkane, then the shorter alkyl group and the Ether group is treated as side chain and prefixed with its binding position on the main chain.
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Chapter 13 Solutions
Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion
- (b) Provide the number of peaks in each of the indicated signals ('H NMR) for the compound below. CH3 6 1 H&C. C H₂ H2 3 HA 2 2 4 5 5arrow_forward8. The emission spectrum below for a one-electron (hydrogen-like) species in the gas phase shows all the lines, before they merge together, resulting from transitions to the ground state from higher energy states. Line A has a wavelength of 10.8 nm. BA Increasing wavelength, \ - a) What are the upper and lower principal quantum numbers corresponding to the lines labeled A and B? b) Identify the one-electron species that exhibits the spectrum.arrow_forwardShow work with explanation....don't give Ai generated solutionarrow_forward
- 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 3arrow_forward2) (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.arrow_forwardDon't used hand raitingarrow_forward
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