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- Given that five isomeric compounds (A, B, C, D, E) with the molecular formula C5H10O were subjected to chemical tests after undergoing Clemmensen reduction compounds A,B, and C all yielded n-pentane, the results of these tests are provided in the table below. Can you draw the structures of compounds A to E based on the outcomes of the chemical tests?Give the series of reactions below, identify and give the iupac name for the following compounds, in short identify and name A,B,CWrite the mechanism of the hydratioin reaction for an alkene, Include arrows, charges and sterochemistry
- (a) Indicate the following alkenes in order of increasing stability. Justify your answers.Question: What is the principle behind the Markovnikov's rule in the addition of HX (where X is a halogen) to an alkene, and what is the exception to this rule?Write a structural formula and give two acceptable IUPAC names for each alkene of molecular formula C7H14 that has a tetrasubstituted double bond.
- 1. what are the differences between acyclic and cyclic forms in terms of their physical properties? 2. what is the role of vinegar in liquid-liquid extraction?What is going on from compound B to compound C? Can you please select all the options that applyOn the line drawn below, provide the systematic (IUPAC) name for the following structure. Be sure to include stereochemistry (R/S, cis-trans, or E/Z) when appropriate.
- Write structures for products A, B, C, and D, showing stereochemistry.Acid-catalyzed dehydration of 2,2-dimethyl-1-hexanol gave a number of isomeric alkenes including 2-methyl-2-heptene as shown in the following equation.(a) Write a stepwise mechanism for the formation of 2-methyl-2-heptene, using curved arrows to show the flow of electrons. (b) What other alkenes do you think are formed in this reaction?Write structures for products A, B, C, and D showinf stereochemistry. (Hint: B and D are stereoisomers)