2. Assign the absolute (R or S) configuration to each stereocenter in the molecules depicted below. Note: assigning R/S configurations to achiral carbons is a "wrong" thing to do! Same extruct out centers orientation sume R confiquation ido opposite confiquration eldoble Switch dE"d"out DARN! (S CI Bril R CI 2 = 17

Organic Chemistry Маxwell Draw the organic and inorganic products for the following acid/base reaction. H .N. Н. 2 products H.

Data for Problem 2 ZOO 180 150 120 140 100 80 770 дом -8 60 40 20 10 9 a 5 015 100 80 Relative Intensity 8 ส 20 20 40 50 ppm septet 3 2 60 70 80 90 100 m/z

Organic Chemistry 1 Here is the professor's solution to the problem. The assignment has been turned in and the answer key has been shared with the class. So, this is the official answer key. However, I do NOT understand the solution. Please explain the answer in a clear step-by-step fashion to me. Explain the answer provided in the image in a clear fashion and as if I did not know much about organic chemistry. Question: Identify the isomeric relationship between the molecules of each pair depicted below. Your choices are diastereomers, enantiomers, identical, or constitutional. Explain your answer without using Fischer projections.

Organic Chem.  This CANNOT be hand-drawn, explanation and illustrations must be typed or digital. if it is hand-drawn your answer will be incomplete and marked as wrong. Molecule: Benzocaine List and explain common industrial or medical applications. what ways can you synthesize this? identifyand discuss the differences. List out any specificprocedural details. Describe the theories behind any method used in asynthesis to create this molecule. (Reactions, techniques,instrumentation, etc.).■For example, if distillation could be used to purify your product, why.

10. Your plane crashes in the Rocky Mountains. Miraculously you survive, and find yourself stranded on a deserted mountain slope. While out gathering berries, you stumble across an abandoned but well-stocked organic laboratory! Mentally thanking your chemistry teacher, you immediately begin making the useful compounds listed below. (Show equations with structures and names and give type of reaction) a) octyl methanoate (a hut deodorizer which smells like oranges) Type of Reaction: Structures and Names:

4. Below are the structures of some medications. Circle and identify functional groups in the structures. H₂C H₂C core MDPV Mephedrone 'N H CH3 Cocaine CH3 CH3 Methylone CH3 Aom CH3 CH3 CH3 Amphetamine NH₂ но... HO HO LaH O ACO OH 10-deacetylbaccatin III

From what we know today, what do the two Kekulé structures for benzene really represent? August Kekulé was the first person to propose a viable structure for benzene in 1865. Structures that can be separated at low enough temperatures (near absolute zero). Structures that are in a state of rapid equilibrium. O Structures that are in resonance. Structures that are conjugated trienes (--C=C--C%3DC--C3C--).

ОН MCPBA NaHCO3, H₂O 1) Dicyclohexylborane 2) NaOH, H2O2

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