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(a)
Interpretation:
From the given set of
Concept introduction:
Alkene Metathesis or olefin metathesis
This breaks the double bond of an alkene and then rejoins the fragments.
When the fragments are joined, the new double bond is formed between two
Terminal alkene gives the best yields of a single alkene product in metathesis because one of the products is ethane, which is equally removed from the reaction mixture, thus shifting the equilibrium in favor of the other new alkene product.
(b)
Interpretation:
The suitable alkenes should be identified which is used in metathesis reaction.
Concept introduction:
Alkene Metathesis or olefin metathesis
This breaks the double bond of an alkene and then rejoins the fragments.
When the fragments are joined, the new double bond is formed between two
that were not previously bonded . Alkenes also undergoes metathesis.
Terminal alkene gives the best yields of a single alkene product in metathesis because one of the products is ethane, which is equally removed from the reaction mixture, thus shifting the equilibrium in favor of the other new alkene product.
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Chapter 11 Solutions
Student's Study Guide and Solutions Manual for Organic Chemistry
- 16. The proton NMR spectral information shown in this problem is for a compound with formula CioH,N. Expansions are shown for the region from 8.7 to 7.0 ppm. The normal carbon-13 spec- tral results, including DEPT-135 and DEPT-90 results, are tabulated: 7 J Normal Carbon DEPT-135 DEPT-90 19 ppm Positive No peak 122 Positive Positive cus и 124 Positive Positive 126 Positive Positive 128 No peak No peak 4° 129 Positive Positive 130 Positive Positive (144 No peak No peak 148 No peak No peak 150 Positive Positive してしarrow_forward3. Propose a synthesis for the following transformation. Do not draw an arrow-pushing mechanism below, but make sure to draw the product of each proposed step (3 points). + En CN CNarrow_forwardShow work..don't give Ai generated solution...arrow_forward
- Label the spectrum with spectroscopyarrow_forwardQ1: Draw the most stable and the least stable Newman projections about the C2-C3 bond for each of the following isomers (A-C). Are the barriers to rotation identical for enantiomers A and B? How about the diastereomers (A versus C or B versus C)? enantiomers H Br H Br (S) CH3 H3C (S) (R) CH3 H3C H Br A Br H C H Br H3C (R) B (R)CH3 H Br H Br H3C (R) (S) CH3 Br H D identicalarrow_forwardLabel the spectrumarrow_forward
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