5. Which of the compounds below would have a lower melting point? Circle your answer and explain why in 1-2 sentences. ve Y 6. For each pair of molecules below, circle the one that would be more soluble in water. a NH₂ y OH OH OH OH
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- 15. a. Draw two constitutional isomers with the formula CaHsBrCl ( Isomer 1 Isomer 2 b. Describe ALL the intermolecular forces isomer 1 can participate in 16. For the molecule below, OH (a) Circle all functional groups present. (b) Label two of the functional groups next to where you circled them 31. Is this molecule is saturated? Explain your reasoning. нннн Н-с—С—С-с-н H HHHHighlight the atoms or groups that are in hydrophilic portions of this molecule in red. If this molecule does not have hydrophilic portions, check the box below the drawing area. CH₂-CH₂-CH₂- This molecule doesn't have hydrophilic portions. X
- Highlight the atoms or groups that are in hydrophilic portions of this molecule in red. If this molecule does not have hydrophilic portions, check the box below the drawing area. CI-CH₂ Cl -CH-CH₂ CI This molecule doesn't have hydrophilic portions. X 000 Ar H ENOrganic Functional Groups Identifying positions labeled with Greek letters in acids and derivatives If possible, replace an H atom on the a carbon of the molecule in the drawing area with a methyl group substituent, and replace an H atom on the ß carbon with a hydroxyl group substituent. If one of the substituents can't be added for any reason, just don't add it. If neither substituent can be added, check the box under the drawing area. HO. Oneither substituent can be added. D X 1/5 0:0 Tyler V ola ArOrganic Functional Groups Identifying positions labeled with Greek letters in acids and derivatives If possible, replace an H atom on the a carbon of the molecule in the drawing area with a methyl group substituent, and replace an H atom on the ß carbon with a hydroxyl group substituent. If one of the substituents can't be added for any reason, just don't add it. If neither substituent can be added, check the box under the drawing area. HO Oneither substituent can be added. OH 0/5 X
- Question 1: How many H- types do each of the following compounds have? Label them a, b, c, etc . In each , circle the hydrogen type you expect to be the most downfield. Please answer for all 4 parts of the question. Thank you for your help!4. Start with NH3 and show step-by-step how the compound N-sec-butyl-N-isopropyl-3-pentanamine can be formed. Draw and name the reactants and products in each reaction (3 separate reactions.) 5. Salicylic acid (shown below) is a polyfunctional molecule (contains more than one functional group.) Circle and identify the functional groups on salicylic acid. Salicylic acid can react with ethanoic acid (acetic acid) to form aspirin. It can also react with ethanol to form ethyl salicylate, a compound with a minty smell used in perfume and artificial flavors. Draw out structures to illustrate each of these reactions. Discuss how these two reactions are similar and how they are different. HO, HOHighlight the atoms or groups that are in hydrophilic portions of this molecule in red. If this molecule does not have hydrophilic portions, check the box below the drawing area.' HO OH This molecule doesn't have hydrophilic portions. OH
- Are these 1-hexanol or 2-hexanol? Please help. I can't seem to figure it out, because when compared around it seems like it could be either.Highlight the atoms or groups that are in hydrophilic portions of this molecule in red. If this molecule does not have hydrophilic portions, check the box below the drawing area.Find the correct answers. Choose. H3C H. Choose. an aldehyde with 2 carbon an alcohol with 3 carbon An alcohol with 4 carbon A ketone with 3 carbon A ketone with 2 carbon он An alcohol with 2 carbon Choose.