Desu Organic Chemistry Homework

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Chapter 15 Homework Answers. 1. Starting from cyclohexene, show how 1,6-hexanediol might be prepared. 2. Using multiple Grignard reactions, show how 4-ethyl-4-heptanol can be prepared using 1-propanol as the only carbon source.

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Electrophilic Aromatic Substitution. 2. • Arene (Ar-H) is the generic term for an aromatic hydrocarbon – The aryl group (Ar) is derived by removal of a hydrogen atom • Aromatic compounds undergo electrophilic aromatic substitution (EAS) – The electrophile has a full or partial positive charge.

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Department of Chemistry Office: SCS Rm 326 Lab: SCS Rm 305 302.857.6534 kmilligan [at] desu.edu. Education. Triple Alumna of Delaware State University. Doctor of Philosophy (Ph.D) in Applied Chemistry. Master of Science (M.S.) in Biological Sciences. Bachelor of Science (B.S.) in Chemistry. Technical Skills

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Chapter 18 Homework. Write a complete mechanism for a directed aldol condensation between cyclohexanone (as the enolate) and pentanal. 2. Number the carbons in 2,6-heptanedione and then apply the same numbers to identify the carbons in each of two possible intramolecular aldol products (after dehydration). Indicate which would be expected to be the major product.

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(1) When the carbocation formed from an alkyl halide, alkene, or alcohol can rearrange to form a more stable carbocation, it does so. (2) FC reactions give poor yields when powerful electron withdrawing groups are present in the aromatic ring, or when the ring bears an -NH₂, -NHR, or -NR₂

Chapter 18 Homework. Write a complete mechanism for a directed aldol condensation between cyclohexanone (as the enolate) and pentanal. 2. Number the carbons in 2,6-heptanedione and then apply the same numbers to identify the carbons in each of two possible intramolecular aldol products (after dehydration). Indicate which would be expected to be the major product.

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