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- 4) (6 pts) a) Chlorocyclopentane may be synthesized two different ways. Fill in the missing reactant required for each pathway. Ch, CI HCI light b) Which reaction represents the more efficient way to synthesize chlorocyclopentane? Briefly explain your choice.Which of the following aldehydes has the highest solubility in water? A) CH₃CH₂C(=O)H B) CH₃CH₂CH₂CH₂C(=O)H C) CH₃(CH₂)₅C(=O)H D) CH₃(CH₂)₁₀C(=O)H E) All of these have equal solubility.13. What is the major organic product of the following reaction? (3 pts) 1, NABH4 2. H30* 14. What is the major organic product of the following reaction? (3 pts) 1, NaBH4 2. H20 15. What is the major organic product of the following reaction? (3 pts) 1. LDA/THF 2. CH3-I 16. Give the major organic products for the following reaction: (2 pts each) 1. CH2=CH-C-H Trace H* 2. HCI, H20
- Draw the principal organic product for the reaction of 2-bromohexane with lithium in diethyl ether, followed by formaldehyde in diethyl ether, and then followed by dilute acid. Click and drag to start drawing a structure. X A G PWhat is the product of the following reaction? (1 equivalent) OH но ?? catalysis with H* 47When 2-pentene is treated with Cl2 in methanol, three products are formed. Account for the formation of each product (you need not explain their relative percentages).
- When reducing 4-nitrobenzaldehyde to 4-nitrobenzyl alcohol, the reducing agent of choice is LIAIH4 (lithium aluminum hydride) because it reduces the nitro group to an amine. O 1) True O 2) FalseWhat is the reagent that is used for the following conversion CH3CH2CHCH2CH3 CH3CH2CHCH2CH3 Br COOH I) 1-Mg/ether, 2- H3O III) 1- Mg/ether, 2- CO2, H3O I) 1-ОН, 2- СТОЗ IV) LIAIH4, OHa-phellandrene and ß-phellandrene are two isomeric diene-containing terpene compounds isolated from eucalyptus plants that are used in fragrances due to their minty and citrusy odors. Use these two compounds to answer the following two questions: a. The addition of 1 equivalent of bromine at room temperature to the phellandrenes will give three possible di-brominated products. Select either a- or ß-phellandrene for this question and draw it in the left box - you can answer this question with either isomer. Draw all three products in the colored boxes depicted - you do not need to depict newly formed stereocenters or show mechanisms. OR a-phellandrene B-phellandrene product 1 select either a- or B-phellandrene product 2 Br₂ room temperature 3 possible products (see below) product 3