Most appropriate method for syntheses
cyclopentanol --> 1-ethylcyclopentanol
1-methylcyclohexanol --> 2 methylcyclohexanone
Most appropriate method for syntheses cyclopentanol --> 1-ethylcyclopentanol 1-methylcyclohexanol --> 2 methylcyclohexanone
Which unknown from the list represents the NMR below: -cycloheptanol -1-methylcyclohexanol -cyclohexanol -cyclopentanol -4-methylcyclohexanol 0 0. 8 0.7 UK-D 0.6 0.5 0.4 0.3 0.2 abundance 0.1 0 90.0 80.0 70.0 60.0 50.0 10.0 190.0 180.0 170.0 160.0 150.0 140.0 130.0 120.0 110.0 100.0 132.3 X: parts per Million : 13C 40.0 323 30.0 20.0 298 27.5
8. Describe the best method for each of the following laboratory syntheses, given a single reactant. Include why you chose this method in your description. a) 1-butanol converted to butanal b) 1-butanol converted to butanoic acid c) 2-butanol converted to 2-butanone d) 2-butene-1-ol converted to 2-butenal e) 2-butene-1-ol converted to 2-butenoic acid f) 1-methylcyclohexanol converted to 2-methlycyclohexanone (this is a multi-reaction process)
Which of the following compounds DO NOT contain a plane of symmetry? (i) cis-1,2-difluorocyclobutane (ii) (R)2-bromo-2-methylcyclohexanone (iii) 4-bromocyclohexanol (iv) cis-3,4-dimethylcyclopentanone (v) 4-methylcyclohexanol
Construct a three-step synthesis of 1,2-epoxycyclopentane from cyclopentanol by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used. Reactant Final Product (cyclopentanol) Reagent 1rightarrow Step 1 Product Reagent 2rightarrow Step 2 Product Reagent 3rightarrow (1,2-epoxycyclopentane)
Experiments Dehydration of 2-methylcyclohexanol Questions 1. Please answer this question on notebook paper, not in the lab sometimes dimicult to read.) tebook (carbon copies are Consider the phosphoric acid-catalyzed dehydration of the following list of nine alcohols. Give the structure of each alcohol and that of the resultant alese. If a MIXTURE of alenes is anticipated. give both products and circle the major product (a) Cyclohexanol: (b) 1-methylcyclohexanol (c)2-methylcobecnold 3-methylcyclohexanol: (e) 4-methylcyclohexanol: (cyclopentanol (R) 3- canotth) 2-pentano: 0) 3-pentanol. 2....
1. starting with 1-methylcyclohexene show synthesis of 2-methylcyclohexanone 2. show the major product for the reaction between Br2/FeBr3 and benzene. Additionally outline a detailed mechanism for the formation of the product.
For 1 - 3, design reasonable syntheses of each of the target molecules using the provided starting material and organic and inorganic reagents of your choice. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Please put all your answers on this sheet. Write your answers like this (actual number of starting steps may vary)material reagent(s) reagent(s) ABCD target Two equally reasonable routes are possible Can you find them both? (For...
PROBLEM 5 Show how you would convert 1-methylcyclopentanol to 2-methyl cyclopentanol
In most situations, you should first figure out the most appropriate valuation method, and then rely entirely on the answer from that method, since it will give you the most accurate estimate of the true valuation. True False
syntheses 7-12. Syntheses: provide the product(s): он РСС , но* CH,Cl2 Brz 1. Brz/PBrg OH 2. H20 NaOH/HO 1. NaOCH2CH3 2. H307 1. (CH3CH2CH2)2Culi 2. Hz0