ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT
ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT
2nd Edition
ISBN: 9781119288510
Author: Klein
Publisher: WILEY
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Chapter 7, Problem 76IP

(a)

Interpretation Introduction

Interpretation: The mechanism for the given reaction should be explained.

Concept Introduction:

SN1 Reaction: It is a nucleophilic substitution reaction in which the rate determining step depends on one reactant. First step is the formation of more stable carbocation which is followed by the attack of nucleophile. Formation of more stable carbocation and the leaving group present in the substrate plays very important role in the reactivity of SN1 reaction. The stability of carbocation is as the following order,

Primary carbocation < secondary carbocation < tertiary carbocation

Carbocation: it is carbon ion that bears a positive charge on it.

Leaving group: it is a fragment that leaves substrate with a pair of electrons via heterolytic bond cleavage.

Nucleophile: donates pair of electrons to positively charged substrate resulting in the formation of chemical bond.

Resonance stabilization: Due to the delocalization of electrons within the molecule the overall energy becomes lower and makes the molecule more stable.

IR spectral studies: It is one of the spectroscopic techniques, used to determine the functional group present in the sample of given compound.

NMR Spectroscopy: It is one of the spectroscopic techniques that determine the properties of atoms and molecules of a given compound by using nuclear magnetic resonance.

Nuclear Magnetic Resonance: When nuclei of given compound sample is subjected to magnetic field, the nuclei absorb and emit the radiation with respect to strength of the field applied.

(b)

Interpretation Introduction

Interpretation: The reactivity for the products formed under given cases are should be explained.

Concept Introduction:

SN1 Reaction: It is a nucleophilic substitution reaction in which the rate determining step depends on one reactant. First step is the formation of more stable carbocation which is followed by the attack of nucleophile. Formation of more stable carbocation and the leaving group present in the substrate plays very important role in the reactivity of SN1 reaction. The stability of carbocation is as the following order,

Primary carbocation < secondary carbocation < tertiary carbocation

Carbocation: it is carbon ion that bears a positive charge on it.

Leaving group: it is a fragment that leaves substrate with a pair of electrons via heterolytic bond cleavage.

Nucleophile: donates pair of electrons to positively charged substrate resulting in the formation of chemical bond.

Resonance stabilization: Due to the delocalization of electrons within the molecule the overall energy becomes lower and makes the molecule more stable.

IR spectral studies: It is one of the spectroscopic techniques, used to determine the functional group present in the sample of given compound.

NMR Spectroscopy: It is one of the spectroscopic techniques that determine the properties of atoms and molecules of a given compound by using nuclear magnetic resonance.

Nuclear Magnetic Resonance: When nuclei of given compound sample is subjected to magnetic field, the nuclei absorb and emit the radiation with respect to strength of the field applied.

(c)

Interpretation Introduction

Interpretation: The IR spectral studies for the products formed under given cases are should be explained.

Concept Introduction:

SN1 Reaction: It is a nucleophilic substitution reaction in which the rate determining step depends on one reactant. First step is the formation of more stable carbocation which is followed by the attack of nucleophile. Formation of more stable carbocation and the leaving group present in the substrate plays very important role in the reactivity of SN1 reaction. The stability of carbocation is as the following order,

Primary carbocation < secondary carbocation < tertiary carbocation

Carbocation: it is carbon ion that bears a positive charge on it.

Leaving group: it is a fragment that leaves substrate with a pair of electrons via heterolytic bond cleavage.

Nucleophile: donates pair of electrons to positively charged substrate resulting in the formation of chemical bond.

Resonance stabilization: Due to the delocalization of electrons within the molecule the overall energy becomes lower and makes the molecule more stable.

IR spectral studies: It is one of the spectroscopic techniques, used to determine the functional group present in the sample of given compound.

NMR Spectroscopy: It is one of the spectroscopic techniques that determine the properties of atoms and molecules of a given compound by using nuclear magnetic resonance.

Nuclear Magnetic Resonance: When nuclei of given compound sample is subjected to magnetic field, the nuclei absorb and emit the radiation with respect to strength of the field applied.

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Students have asked these similar questions
Can you please help mne with this problem. Im a visual person, so can you redraw it, potentislly color code and then as well explain it. I know im given CO2 use that to explain to me, as well as maybe give me a second example just to clarify even more with drawings (visuals) and explanations.
Part 1. Aqueous 0.010M AgNO 3 is slowly added to a 50-ml solution containing both carbonate [co32-] = 0.105 M and sulfate [soy] = 0.164 M anions. Given the ksp of Ag2CO3 and Ag₂ soy below. Answer the ff: Ag₂ CO3 = 2 Ag+ caq) + co} (aq) ksp = 8.10 × 10-12 Ag₂SO4 = 2Ag+(aq) + soy² (aq) ksp = 1.20 × 10-5 a) which salt will precipitate first? (b) What % of the first anion precipitated will remain in the solution. by the time the second anion starts to precipitate? (c) What is the effect of low pH (more acidic) condition on the separate of the carbonate and sulfate anions via silver precipitation? What is the effect of high pH (more basic)? Provide appropriate explanation per answer
Part 4. Butanoic acid (ka= 1.52× 10-5) has a partition coefficient of 3.0 (favors benzene) when distributed bet. water and benzene. What is the formal concentration of butanoic acid in each phase when 0.10M aqueous butanoic acid is extracted w❘ 25 mL of benzene 100 mL of a) at pit 5.00 b) at pH 9.00

Chapter 7 Solutions

ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT

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