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Concept explainers
(a)
Interpretation:
The sequence of arrow-pushing pattern in the given multi step reaction has to be identified.
Concept Introduction:
Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.
There are only four characteristic patterns, and all ionic mechanisms are simply combinations of these four steps, and they are,
- (1) Nucleophilic attack
When we identify a nucleophilic site and an electrophilic site, the arrow in the mechanism step shows the nucleophile attacking.
- (2) Proton transfer
- (3) Loss of leaving group
- (4) Rearrangements
Rearrangements will always occur when an alkyl group or hydrogen can shift to form a more stable carbocation. There are mainly two types of rearrangement shifts and they are,
Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.
Curved arrows used to understand a reaction mechanism.
Curved arrows are drawn to show how the electrons move as new covalent bonds are formed existing covalent bonds are broken.
Each arrow represents the simultaneous movement of two electrons from a nucleophile towards an electrophile.
Nucleophile: It is negatively charged species which seeks for positive charge and hence donate pair of electrons to positively charged species (electrophiles) which results in the formation of
(b)
Interpretation:
The sequence of arrow-pushing pattern in the given multi step reaction has to be identified.
Concept Introduction:
Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.
There are only four characteristic patterns, and all ionic mechanisms are simply combinations of these four steps, and they are,
- (1) Nucleophilic attack
When we identify a nucleophilic site and an electrophilic site, the arrow in the mechanism step shows the nucleophile attacking.
- (2) Proton transfer
- (3) Loss of leaving group
- (4) Rearrangements
Rearrangements will always occur when an alkyl group or hydrogen can shift to form a more stable carbocation. There are mainly two types of rearrangement shifts and they are,
Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.
Curved arrows used to understand a reaction mechanism.
Curved arrows are drawn to show how the electrons move as new covalent bonds are formed existing covalent bonds are broken.
Each arrow represents the simultaneous movement of two electrons from a nucleophile towards an electrophile.
Nucleophile: It is negatively charged species which seeks for positive charge and hence donate pair of electrons to positively charged species (electrophiles) which results in the formation of chemical bond.
(c)
Interpretation:
The sequence of arrow-pushing pattern in the given multi step reaction has to be identified.
Concept Introduction:
Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.
There are only four characteristic patterns, and all ionic mechanisms are simply combinations of these four steps, and they are,
- (1) Nucleophilic attack
When we identify a nucleophilic site and an electrophilic site, the arrow in the mechanism step shows the nucleophile attacking.
- (2) Proton transfer
- (3) Loss of leaving group
- (4) Rearrangements
Rearrangements will always occur when an alkyl group or hydrogen can shift to form a more stable carbocation. There are mainly two types of rearrangement shifts and they are,
Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.
Curved arrows used to understand a reaction mechanism.
Curved arrows are drawn to show how the electrons move as new covalent bonds are formed existing covalent bonds are broken.
Each arrow represents the simultaneous movement of two electrons from a nucleophile towards an electrophile.
Nucleophile: It is negatively charged species which seeks for positive charge and hence donate pair of electrons to positively charged species (electrophiles) which results in the formation of chemical bond.
(d)
Interpretation:
The sequence of arrow-pushing pattern in the given multi step reaction has to be identified.
Concept Introduction:
Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.
There are only four characteristic patterns, and all ionic mechanisms are simply combinations of these four steps, and they are,
- (1) Nucleophilic attack
When we identify a nucleophilic site and an electrophilic site, the arrow in the mechanism step shows the nucleophile attacking.
- (2) Proton transfer
- (3) Loss of leaving group
- (4) Rearrangements
Rearrangements will always occur when an alkyl group or hydrogen can shift to form a more stable carbocation. There are mainly two types of rearrangement shifts and they are,
Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.
Curved arrows used to understand a reaction mechanism.
Curved arrows are drawn to show how the electrons move as new covalent bonds are formed existing covalent bonds are broken.
Each arrow represents the simultaneous movement of two electrons from a nucleophile towards an electrophile.
Nucleophile: It is negatively charged species which seeks for positive charge and hence donate pair of electrons to positively charged species (electrophiles) which results in the formation of chemical bond.
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Chapter 6 Solutions
Organic Chemistry Third Edition + Electronic Solutions Manual And Study Guide
- Draw the curved-arrow mechanism with the drawings of the molecules, not just abbreviations. -NO₂ Sn, HCl (aq) E D H (CH3CO)₂O -NH2 CH3arrow_forwardWhat is/are the product(s) of the following reaction? Select all that apply. * HI A B C OD OH A B OH D Carrow_forwardIn the image, the light blue sphere represents a mole of hydrogen atoms, the purple or teal spheres represent a mole of a conjugate base. A light blue sphere by itself is H+. Assuming there is 2.00 L of solution, answer the following: The Ka of the left & right solution is? The pH of the left & right solution is? The acid on the left & right is what kind of acid?arrow_forward
- 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.arrow_forwardQuestion 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 OAarrow_forwardNonearrow_forward
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