H3C-OHO!!!!Select to DrawOHOHOHPlease select a drawing or reagent from the question areaIncorrect, 1 attempt remainingYour structure is missing one or more chiral centers OR the relativeorientation of a stereocenter(s) (chiral center(s)) is not shown. Use adash or wedge bond to indicate the relative orientation of substituentswhere applicable. Review the chemical name and/or reaction conditionspresented. If a reaction is taking place, only the atoms and bondsinvolved in the reaction will undergo a stereochemical change.Retry The southern pine beetle utilizes a multi-componentaggregation pheromone (one component shown below) to startmass colonization of healthy trees. The biosynthetic pathwayinvolves the cyclization of this acetal from the straight chainstructure. Draw the straight chain structure that could be usedto form this acetal. Use wedges and dashes to correctly depictthe stereochemistry.H3C-OH✔

Acetals are generally formed during the interaction of carbonyl bond (C=O) with a hydroxyl group…

The southern pine beetle utilizes a multi-component aggregation pheromone (one component shown below) to start mass colonization of healthy trees. The biosynthetic pathway involves the cyclization of this acetal from the straight chain structure. Draw the straight chain structure that could be used to form this acetal. Use wedges and dashes to correctly depict the stereochemistry. H3C OH

The southern pine beetle utilizes a multi-component aggregation pheromone (one component shown below) to start mass colonization of healthy trees. The biosynthetic pathway involves the cyclization of this acetal from the straight chain structure. Draw the straight chain structure that could be used to form this acetal. Use wedges and dashes to correctly depict the stereochemistry. H3C OH

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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Click the "draw structure" button to launch the drawing utility. Compounds that contain both carbonyl and alcohol functional groups are often more stable as cyclic hemiacetals or cyclic acetals than as open-chain compounds. The following is an example of such a compound. Deduce the structure of the open-chain form of the compound. CH3CH2 CH3 Brevicomin (sex attractant of Western pine beetle)
Either the reactant (X) or the major organic product is missing from the equation below. Draw the missing compound. X + H₂ Pd/C CH3 CH₂CHCHCHCH3 CH3 H3C
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