Safari File Edit View History Bookmarks Window Help -97% Thu 11:27 AM Q E cvg.cengagenow.com Cengage OWLv2 | Online teaching and learning resource fro... ketone - Google Search Draw the structures of 4 aldehydes with formula... Chapter 2 EOC Question 2 1 pt Question 31 pt Question 41 pt Question 51 pt Question 6 Question 7 Question 8 Question 9 Question 10 Question 11 Question 12 Question 13 Question 14 Question 15 Question 16 Question 17 30 Draw the structures of 4 esters with formula C4Hgo2 200615 486312 4869...54 n.jpg You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu 9ee6b- 00x.jpg C P 1 pt 1 pt 1 pt 599563 486312 15357...39 n.jpg 1 pt 1 pt 1 pt 1 pt ChemDoodle 31-10 1024x1024 ProgresS 5/17 items Due Feb 8 at 11:00 AM Submit Answer Try Another Version 1 item attempt remaining Previous Next creen Shot -01...9.24 AM Finish Assignment Email Instructor Save and Exit 1,308

Carbocations rearrange with some ease. An example of this is shown below. Indicate, with the corresponding arrows, how this process occurs. The carbocation 2 is more stable than 1, why is this? Explain it using (drawing) structures.

1. Using Br2 in C2H4Br2 will result in HBr and ______. a. C2H3Cl3 b. C2H4Cl3 c. C2H2Cl3 d. none of the above   2. How many halogenation are posible in propane? a. 3 b. 8 c. 6 d. 10   3.Sulfonation of pentane will result in ________ and water. a. C5H11SO3H b. C5H12SO3H c. C5H14SO3H d. none of the above   4.Nitration of hexane will result in ________ and water. a. C6H13SO3H b. C6H15NO2 c. C6H13NO2 d. C6H14NO2   5.How many moles of O2 in heating a C12H26 (dodecane) a. 27 b. 37 c. 24 d. none of the above

Consider the following aromatic compounds a para-substituted compound?, the most reactive towards EAS? an ortho-substituted compound? does not react with RX, FeX3?

Knowing the properties of organic molecules, students will now design experimental set-ups that will maximize the yield and purity of the target organic molecule. The students must prove that their choice of materials is available for purchase by providing a CAS number or a catalogue from a supplier (example: Sigma Aldrich). Also, included in this part is the discussion of the Chemistry behind the synthesis as well as safe laboratory techniques and practices to synthetic design.

Just number 6 and also include a 2-D version of each of the structures.

Draw the most stable carbocation that can be formed by the compound in Figure 5. [Generate a SMILES notation: https://jsme-editor.github.io/dist/JSME_test.html. Copy the notation (CTRL+C) and paste it as the answer to this question (CTRL+V).] *

What is the value in kJ/mol, of the lowest energy trnasition above?  a.) 545 b.) 444 c.) 320 d.) 266

Explain briefly and clearly the following concepts, taking as reference the molecule of n-butane and the corresponding drawings or illustrations. See pages 149-152 of the book Organic Chemistry, sixth edition (J. G. Smith). 4. What is steric hindrance in a conformation? Then draw a picture to illustrate the concept?  5. What is the torsional stress of a conformation? Then draw a picture to illustrate the concept?  6. Describe 1,3-diaxial interaction and illustrate with a specific example.

Consider the compounds 1-pentanol,CH3-CH2-CH2-CH2-CH2-OH, melting point -78C boiling point 138C, MW=88.15. 1,6-hexanediol ,HO-CH2-CH2-CH2-CH2-CH2-CH2-OH, mp 42C,bp=250C.MW=118.18. The compound 1,6-hexanediol is more soluble in water than 1-pentanol is. This is because 1,6-hexanediol.... 1) has more carbon atoms 2)has a higher molecular weight  3)has more -OH groups 4)is a solid at room temperature