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2. Starting Molecule 2-methylbutane Target Molecules 6-methyl-3-octanone and 6-methyl-4-octanone сн, Н,с сн, and
е CH с 3 н нн СН з ХotHr CH 3 Н. a I Question 12 1 pts The two methyl groups in the molecule are... Homotopic Enantiotopic Diastereotopic Heterotopic
Problem #3 Provide full IUPAC names for each molecule below: CH н,с сн,
e сн, осн, снснснснсн,сн, CH снснснснсн,сн, осн, сн, с сн Cla сн-снсн-снсH,сн, снрн When 2-methyl-3. besene is treated with Cly in methanol, three products are formed (neglecting stereohomers). Draw curved arrews to show the movement of electroas in this step of the reaction mechanism Arrow paching Instructions но— сн, :б—сн, CH :0- сн На -C-CH Cн но — сн, Н,с- CH Нас —с Sab A Ery Anoe rs
14. (1 pt each) Name the following molecules. CH3 CH3 нно н н-с-с-с-NA ті Hн н,с Сн, Н CH,CH нс H 15. (3 pts each) Give the product(s) for the following reactions, and name all reactants and products. CH, он ОН н,с + нэс- сн - сн 3 нус. NH2 ОН Hн ІІ ОН + н-с-с-о-н НО P н Н ОН
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
Question 3 (2 points) Choose the best name for the compound drawn. 6-methyl-3-propyl-2-heptanal 2-methyl-5-octanone 6-methyl-3-propyl-2-heptanone 3-isopentyl-2-hexanone
The reaction is: 2-methyl-2-butanol + HCl -->
2-chloro-2-methylbutane via an SN1 reaction.
Experiment 4: Synthesis of a tertiary alkyl halide Page 3 of 6 Distillation is a technique that is to purify liquid compounds. Use theoretical data to explain how distillation is used to separate the target product in this reaction from any residual unreacted starting material in the reaction. [2 marks]
Please answer all Naming
Identify the following molecule: a. 2-ethylbutane b. 2-methylbutane c. 3-methylbutane d. 3-methylpentane Identify the following molecule: a. 2-dimethylbutane b. 2, 2-dimethylhexane c. 2-dimethylpentane d. 2, 2-dimethylpropane Identify the following molecule: a. 2-methyl-4-ethylheptane b. 4-ethyl-6-methylpentane c. 4-ethyl-2-methylheptane d. 4-ethyl-3-methyloctane Identify the following molecule: a. 5-ethyloctane b. 4-butyloctane c. 5-methyloctane d. 4-propyloctane Identify the following molecule: a. 1, 2, 3, 4-tetraethylbutane b. 2, 3-tetraethylbutane c. 2, 3-tetramethylbutane d. 2, 2, 3, 3-tetraethylbutane
For the reaction below, focus only on 2-methyl-2-butanol
(starting material) and 2-chloro-2-methylbutane (desired product).
We will not analyze HCl or H2O by IR.
From the two IR spectra below, identify which spectrum belongs
to which molecule. Then label the IR spectrum with the molecule’s
characteristic IR peaks. Highlight or place a box around the most
characteristic peak in the starting material’s IR. You do not need
to label the fingerprint region.
For the reaction below, focus only on 2-methyl-2-butanol...
provide a synthesis for the target molecule shown.
н" TM SM Bonus: (10 pts) Starting from Benzene and using reagents that we have discussed in class, design a sy molecule (TM).