Please answer all of them 7. For the terpene biosynthesis shown below, use arrow-pushing to depict the carbon-carbon bondformation or "head-to-tail" coupling of the five carbon building blocks. Remember that thepyrophosphate leaving group must be activated by a metal, so use Mg²+.OPPOPPOPP =V. SYNTHESIS Complete the syntheses below by showing all intermediate compounds, all necessaryreagents/conditions/work-up steps. Each synthesis requires multiple steps. To receive full credit, theconditions and order of steps must maximize selectivity for the desired product.1. Provide ALL the appropriate reagents or the CORRECT products in the sequence below.Br2, FeBr31. H₂CMgBr2. H₂0+H3CCH₂ OHOOHPdCl₂(PPH3)2Na₂CO31. SOCI₂2. FeCl32. Perform a retrosynthesis that illustrates how the compound below could be prepared from chlorobenzene.Include all reagents and intermediate compounds.NO₂ÖHCO₂HCI

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Chemistry

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Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Question

Please answer all of them

7. For the terpene biosynthesis shown below, use arrow-pushing to depict the carbon-carbon bond
formation or "head-to-tail" coupling of the five carbon building blocks. Remember that the
pyrophosphate leaving group must be activated by a metal, so use Mg²+.
OPP
OPP
OPP =
V. SYNTHESIS Complete the syntheses below by showing all intermediate compounds, all necessary
reagents/conditions/work-up steps. Each synthesis requires multiple steps. To receive full credit, the
conditions and order of steps must maximize selectivity for the desired product.
1. Provide ALL the appropriate reagents or the CORRECT products in the sequence below.
Br2, FeBr3
1. H₂CMgBr
2. H₂0+
H3C
CH₂ OH
O
OH
PdCl₂(PPH3)2
Na₂CO3
1. SOCI₂
2. FeCl3
2. Perform a retrosynthesis that illustrates how the compound below could be prepared from chlorobenzene.
Include all reagents and intermediate compounds.
NO₂
ÖH
CO₂H
CI

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