**Stereochemistry and Combustion Reactions: Questions and Activities**2. **Stereochemistry** - (A) Draw 1-bromo-1-ethanol in 3 dimensions. - (B) Draw 1-bromo-1-ethanol in a Fischer projection. - (C) Next to your molecules in Part A and Part B, draw the enantiomers.3. **Complete Combustion of Propane** - If 2 moles of propane undergo complete combustion, how many grams of carbon dioxide are produced?4. **Combustion Reaction Balancing** - When one mole of propane undergoes complete combustion with oxygen gas, what are the products? Write the balanced equation reaction and show all your work.

Since you asked multiple questions so as per Q&A guidelines of portal I solved first question…

Answered: 2 Stereochemistry 1 Draw 1-bromb - 1.…

2 Stereochemistry 1 Draw 1-bromb - 1. ethanol in 3 dimensions Boraw 1-bromo -1- thanse in a Fischer projection Next to your molecules in Part A and Part B draw the enantiomers

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...

See similar textbooks

Similar questions

Draw the major product as a planar projection (not chair conformation) for the E2 reaction shown. Do not include stereochemical configurations for the chirality centers. Draw the product. H H H. H- -CH, но- H3C. -CI DMSO CH3 H The E2 reaction involves a concerted removal of a B-hydrogen and the chlorine. Note: The chlorine and B-hydrogen must be in an anti-periplanar relationship to each other. Notice you will have to flip the conformation of the cyclohexane ring to achieve this relationship.
HD V/ CH3-C-CH- CI a) Draw the R, R stereoisomer of the molecule shown below. b) Draw the two Newman projections that show the anti-periplanar geometry required for E2 elimination of the molecule in part a). c) Draw the products of E2 elimination of the molecule in part a) and indicate the stereochemistry (E or Z).
HO. HO OH a. What pharmacological effects would the product elicit? b. In what plant does this compound occur naturally? OH HN NH₂ CF3 a. How many chiral centers are in the product? b. How would you specifically isolate one of the stereoisomers? c. What is the name of this drug? d. What is the configuration of the active stereoisomer of this drug, R or S?
Glyceraldehyde is shown as a Fischer projection. H. НО -H ČH2OH (a) Identify the stereochemistry configuration: R S
Draw the Newman projection (sighting down this bond) of the conformation that will be capable of an E2 elimination. R/S stereochemistry is graded.
What reagent is needed to convert (CH3)2CHCH2COCl to each compound ?
Draw the product formed (including stereochemistry) in attached pericyclicreaction.
Draw the major product for each of the reactions, showing the correct stereochemistry, if any. Draw hydrogen atoms on chirality centers.
*** khách Predict the major product formed in the following reaction. The starting material is shown as a Fischer projection. CH3 O A 1) B 2) C 3) D 4) SH S 1) H CI CH₂CH3 SH 2) NaSH SH 3) Major product 4) SH
5. For the following transformations draw the product. Draw only one stereoisomer in the box if there is more than one. Provide what type of mixture of products would be obtained (1 chiral compound, enantiomers, diastereomers, achiral). a) b) d) H3C f) CI OH 2. OH 1. NaNH, H3C OH 2. 1. LDA, -78 °C NaOH 1. TsCI, NEt3 2. NaCN 2. CH3 Br 1. SOCI2, NEt3 Br OH RT H₂SO4 heat 1 enantiomer (1 chiral compound) 1:1 mix of enantiomers mixture of diastereomers achiral 1 enantiomer (1 chiral compound) 1:1 mix of enantiomers mixture of diastereomers achiral 1 enantiomer (1 chiral compound) 1:1 mix of enantiomers mixture of diastereomers achiral 1 enantiomer (1 chiral compound) 1:1 mix of enantiomers mixture of diastereomers achiral 1 enantiomer (1 chiral compound) 1:1 mix of enantiomers mixture of diastereomers achiral 1 enantiomer (1 chiral compound) 1:1 mix of enantiomers mixture of diastereomers achiral
Please assign priority groups and assign R or S stereochemistry for each
Designate the following compound as R or S. CH₂CH₂l HO-C-CH3 CH₂OH Select one: O A. There are no stereocenters in molecule. OB. S C. R