4. Consider the following compound with the molecular formula C4H:02: a. Draw a constitutional isomer that you expect w...
Please answer all questions correctly especially question d. Also, explain if you can! Consider the following compound with the molecular formula C4HgO2 OH a. Draw a constitutional isomer that you expect would be approximately one trillion (10) times more acidic than the compound above. What explains the increased acidity of this isomer? Draw a constitutional isomer that you expect will be less acidic than the compound above. Why would the acidity be decreased? b. Draw a constitutional isomer that you...
1. Consider an organic compound with molecular formula C H:02: a) Draw one constitutional isomer that has a very small pka. b) Draw a constitutional isomer that is less acidic than the compound from part a). c) Draw a constitutional isomer that has is more basic than the compound in part b). D J AL . ... .... . . .. . . - Predict the stracture of the product formed in the reaction of 3-(3-5cetyl-5-for myl-4- hydroxy Phenyi) Propohoic...
Please help! 4. Suppose Compound B is the conjugate base of Compound A. Calculate the approximate concentration of Compound A that must be present in a 0.042 M solution of Compound B to produce a pH of 4.96. The K. for Compound A is 1.8 x 109. Show your work. Round your final answer to the nearest hundredth decimal place. (5pts) 5. Consider the structure below. Then using the empty boxes, answer parts (a)-(e). HO (a) (1 pts) Draw a...
1. (6 pts) A compound has a molecular formula of CHO a. Draw a structure of a compound with the above formula that contains an ether group and one chirality Center b. Draw the structure of an ether that is a constitutional isomer of the compound drawn in part above 1 c. Draw the structure of a constitutional isomer of the compound drawn in part (a.) which contains a different functional group.
Draw the structural formula(s) for the branched constitutional isomer(s) with the molecular formula C8H18 that have two methyl groups on different carbons. (Please draw ALL correct & possible structures)
4.) a) (10 pts) Consider the three constitutional isomers of dioxane (C&H:02): One of these constitutional isomers (Isomer A) is stable under basic conditions as well as mildly acidic conditions and is commonly used as a solvent. One of these (Isomer B) is only stable under basic conditions but undergoes hydrolysis under mildly acidic conditions. The remaining isomer (Isomer C) is extremely unstable and potentially explosive. Identify each isomer (label each as A,B or C) and explain the properties of...
Question 1 Draw a bond-line structure for each constitutional isomer with molecular formula C4H100. Include Lone Pairs in your answer. ? Edit By accessing this Question Assistance, you will learn while you earn points based on the Point Po
3B) Draw the constitutional isomers of trimethylcyclopropane as skeletal structures. 3C) For each constitutional isomer you drew in part (a), draw any stereoisomers of that structure, explicitly showing stereochemistry with dash/wedge bonds. Use skeletal structures. 2. This molecule has a ring strain of 70 kl/mol. Circle which type of strain is most important, and explain why you circledit: Angle torsional steric 3. Only one stereoisomer of this compound is stable - draw the relative stereochemistry at the ring Junction with...
Practice Problem 22.41 Draw all constitutional isomers with molecular formula C4H11N, and provide a name for each isomer. Part b Draw the constitutional isomers with a primary amine (RNH2). ? Edit LINK TO TEXT By accessing this Question Assistance, you will learn while you earn points based on the Point Potential Policy set by Parts The parts of this question must be completed in order. This part will be available when you complete the part above.
8.1) 8.5) Give the appropriate IUPAC name for the following structural formula of a halogenated compound. CH3 CI Нас (Where stereochemistry is shown, include a designation of configuration in your answer. Use cis/trans designations only to represent stereochemistry for cyclic compounds. It is not necessary to use italics in writing compound names.) Name: There are five cycloalkanes with the molecular formula C5H10. When treated with chlorine at 300°C, isomer A gives one monochlorination product. Under the same conditions, isomer B...