1. The monochlorination of 2,2-di-methyl-4-methylpentane in the presence of light gives different products. Draw the structures of all, Also, determine which one of those are the major and minor products. Box your answers. Given that the selectivity of Cl towards 1°, 20, 3° hydrogen is 1,4,5, respectively. Show all your detailed work
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- Write the reaction of 1-bromopentane with sodium ethoxide and show all possible products (E2 and SN2) that could occur. Please don't give handwritten eI am given a compound, cis-2-bromo-1-methylcyclohexane and my product is shown to be 3-methyl-1-cyclohexene.Since this is not a Zeitseif product, would it arise through use of a hindered, strong base?Considering the following reaction, while kinetic resolutions limit your yield of, for example, acetate 3 to 50%, in certain cases this can be improved by using a sequence of reactions that convert the undesired enantiomer to the desired one. Propose a series of such reactions that would allow you to convert the (S)-2 to acetate 3. Thank you :)
- Please state which is the main product when 2-methylbuta-1,3-diene reacts with one equivalent of HBr for a limited time below 0 °C?In the chemical reaction between 2-chloro-2-methyl-propane and ethanolic silver nitrate solution, a precipitate is definitely formed. Using the skeletal structures of the molecules, write out the skeletal structure of each reaction (don't include the mechanism). Identify what the nucleophile is in each type of reaction, especially within this SN1 reaction. Explain the reactivity of each electrophile/substrate in terms of whether they are tertiary, secondary, primary, etc. for each reaction. Include the overall chemical reaction.Draw all four products that are expected when 2-ethyl-3-methyl-1,3-cyclohexadiene is treated with one equivalent of HBr at room temperature, and show mechanisms for their formation.For the mechanism, include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly. Do not use abbreviations such as Me or Ph.
- Give a detailed reaction mechanism for the reaction expected to occur when 2-bromo-2-methylpentane is heated with sodium methoxide. Draw clear structural formulas of all relevant species and use curved arrows to represent electron flow. Discuss the stability of the final compoundUsing the reagents listed in the table below, show how to convert 1-pentyne to the following product: (Specify the reagents you would use to carry out the conversion by using letters from the table. The reaction may require more than one step, if so, write the letters in the order that they are used, e.g., hb. If two or more ways of conversion to the same product are possible, show only one of them.)Read these directions carefully. For the reaction of 3-methyl-1-propene with Cl2 and H2O shown below, fill in the details of the mechanism. Draw the appropriate chemical structures and use an arrow to show how pairs of electrons are moved to make and break bonds during the reaction. Be sure to write all lone pairs of electrons and all formal charges. Finally, in the boxes provided by the arrows, write which kind of mechanistic element is being indicated, such as "make a bond", "add a proton", etc.
- Show stereo chemistry and possible outcomes and the steps for the reaction.This is a problem I am struggling with, because I still struggle to understand how to accurately describe why the nitro benzene-type structure is difficult to synthesize. Please help! Also the second problem I am really struggling to put words into a problem in order to solve it. Please show all steps for both 1 and 2!A chemist wanted to determine experimentally the relative ease of removing a hydrogen atom from a tertiary, a secondary, and a primary carbon by a chlorine radical. He allowed 2-methylbutane to undergo chlorination at 300 °C and obtained as products 36% 1-chloro-2-methylbutane, 18% 2-chloro-2-methylbutane, 28% 2-chloro-3-methylbutane, and 18% 1-chloro-3-methylbutane. What values did he obtain for the relative ease of removing a hydrogen atom from tertiary, secondary, and primary hydrogen carbons by a chlorine radical under the conditions of his experiment?