I have multiple questions

Trbetr1004
timer Asked: Oct 19th, 2017

Question Description

I need 3, 4, 5, and 8 completed in the next 11hours

Unformatted Attachment Preview

Assignment 1 (10 pts) 1. Give IUPAC names to these hydrocarbons; also determine the molecular formula for each: 2. Draw structures from these names which are not strictly correct and then give them a correct IUPAC name: 2-ethyl-2-methylpropane 2,3,3-trimethylbutane 3-methyl-4-ethylhexane 2-methyl-4-methylhexane 3. In reading section 12.15, list the 6 products collected by the fractional distillation of crude petroleum shown in the Figure 12.9. 4. For the compounds shown in figure 13.5 (“selected terpenes…”), and in the “Carotenoids: A Source of Color” box, list them in order of number of double bonds. 5. Also from the “Carotenoids” box, what structural feature of these types of molecules gives many organic compounds their distinctive colors? 6. Draw structures from these names which are not strictly correct and then give them a correct IUPAC name: 2-methyl-4-pentene cyclohexene 3-methyl-2,4-pentadiene 3-methyl-3-cyclopentene 1,2-dimethyl-3- Assignment 2 (10 pts) Match each of the following small molecules to its description, and draw the chemical structure to the left of its description: isooctane, acetylene, ethanol, methanol, acetone, acetaldehyde, acetic acid, formic acid, diethylether, ethyl acetate Used for extraction of caffeine from tea and coffee, also main ester present in wine Oxidative product of ethanol and implicated in hangover effects One component from which the octane rating is determined The sting of an ant bite is due to this Present in wine, beer, liquors, vanilla extract Used as an anaesthetic in the past Also called wood alcohol and causes blindness and death if present in alcoholic beverages Present usually ~5% in vinegar and is an oxidative product of ethanol Used in welding torches due to the hot flame it produces Used in nail polish remover and also smelled on the breath of diabetics with ketoacidosis Assignment 3 (10 pts) 1. Draw a chemical structure for each of the following and give them IUPAC names: Chemical formula: Primary alcohol Secondary alcohol Tertiary alcohol Carbon atom ring as part of structure (have to lose 2 H’s from formula…) C5H12O IUPAC name: C4H10O IUPAC name: 2. It is useful to be acquainted with the many terms in common use for various alcohol solutions. Indicate what each common term correlates to in terms of IUPAC names for the alcohols referred to here (or what sort of solution it refers to). • Absolute alcohol • Wood alcohol • Grain alcohol • Denaturated alcohol • Rubbing alcohol • 70-proof alcohol • Drinking alcohol • “alcohol” Give the IUPAC name for each of these alcohols as described: • Major ingredient in most brands of antifreeze • The alcohol present in alcoholic beverages • Often applied to the skin because of its “cooling effects” • Thick liquid that has the consistency of honey 3. Moving on to the next chapter: for section 15.7, on the back of this page make a table or outline summarizing the content of this section to look at important aldehydes and ketones. 4. Take a look ahead to section 23.7, in the diagram: “Summary of the Reaction of the Citric Acid Cycle”. Given one example each from the compounds shown which contains: a secondary alcohol ___________________; a tertiary alcohol _____________________; a ketone ___________________; an alkene_______________ Assignment 4 (10 pts) Draw two examples for each of the following functional groups as shown below. Each should contain 10 carbons and should be a branched compound (challenge yourself a little bit beyond straight chains! But don’t go overboard…). Also give each an IUPAC name. Altogether that will be 10 structures, 10 names. Alkene alkene Alcohol Alcohol Ketone Ketone Aldehyde Aldehyde Carboxylic acid Carboxylic acid Assignment 5 (10 pts) For each of the following, analyze the IUPAC name to correlate it to the chemical structure. We will do the first one in class together. Lyrica: (S)-3-(aminomethyl)-5-methylhexanoic acid Naproxen: (+)-(S)-2-(6-methoxynaphthalen-2-yl) propanoic acid Methadone: 6-(Dimethylamino)-4,4-diphenylheptan-3-one Methoprene: 1-methylethyl-(E,E)-11- methoxy-3,7,11-trimethyl- 2,4-dodecadienoate Salmeterol: 2-(hydroxymethyl)-4-{1-hydroxy-2-[6-(4-phenylbutoxy)hexylamino]ethyl}phenol Metoprolol: 1-(isopropylamino)-3-[4-(2-methoxyethyl)phenoxy]propan-2-ol Assignment 6 (10 pts) Reactions of alkenes, alcohols, aldehydes, ketones, and carboxylic acids, from chapter sections 13.9, 14.9, 15.9, 15.10. a. Cr2O7-2 CH3CH2CH2CH2OH b. H3C CH3 H2 / Pt OH c. H3C C CH3 MnO4- CH3 H2C a. H2 / Pt CHCH2CH2CH2CH3 O d. H3C C H2 / Pt b. O OH H3C H2 / Ni CH2 CH2 C CH3 O H3C f. C CH3 H3C 1. LiAlH4 2.H2O c. OH H+, H2O 2. H2O OH H2SO4, heat d. H3C g. 1. LiAlH4 C O e. CH3CH2CH2CH2OH H3C C CH3 H3C H2SO4, heat O e. Cr2O7 2- C H3C CH3 H+, H2O f. O MnO4g. H3C C OH CH3 h. OH MnO4- Assignment 7 (10 pts) : A family of organic molecules – structure and function Sometimes molecules that have a similar function have similar structures and one way to develop new molecules for pharmaceutical purposes is to make changes in a known molecule that has certain properties, trying to capitalize on properties that are desired and minimize properties that are detrimental. On the other hand, sometimes it is not obvious why structurally dissimilar molecules have the same function, which can raise interesting questions of molecule-protein interactions. Terminology: Define Opioid: Define Opiate: Who was Morpheus?____________________________________________ Draw Morphine here: The biological source of morphine is ___________________________ Using your drawing of morphine, indicate the differences of each of these from morphine: Heroin Codeine Oxycodone These molecules also interact with the opioid receptor, but are not derivatives of morphine; draw their structures here. (Beta-Endorphin is called an endogenous opioid; endogenous means ___________________________________. Its function is:___________________________________________________ ) Fentanyl Tramadol beta-Endorphin (just list amino acids by their three-letter abbreviations) Assignment 8 (10 pts) Stereochemistry: Chapter 18.4-18.7 1. Sort the following according to whether they apply to chiral or achiral molecules: __________Four different groups bonded to the C atom __________Mirror images superimposable __________Can be designated either D or L __________Has optical activity __________Has no optical activity __________Optical activity is 0 __________Its enantiomers have identical bp, mp, density, and solubility 2. Identifying chiral centers: pick two examples of pharmaceutical molecules or molecules from your project which have chiral centers, draw here (or copy-paste), and indicate the chiral centers. 3. For these molecules, decide whether they are D or L, considering whether they are rotated the correct orientation. 4. For the above molecules, draw their enantiomers here 5. Diastereomers with two stereocenters: Draw the remaining stereocenters, and determine which are enantiomers of each others, and which are meso. 6. Determine the number of stereoisomers possible (2n) for the following molecules: compound (section) Nicotine (17.10) Pseudoephedrine (17.10) Quinine (17.11) Cholesterol (19.9) Leukotriene B4 (19.13) # of sp3 stereocenters # of stereoisomers possible Assignment 9 (10 pts) For review and practice (and thinking things through) on carbohydrates, chapter 18. Shown below is a diagram of the equilibrium between the open chain and the pyranose forms of Dglucose. Answer the following questions. CHO H HO CH2OH O H H OH OH H H OH H OH H CH2OH CH2OH H OH H OH OH H O H OH OH H H OH H OH 1. Label the open chain (
User generated content is uploaded by users for the purposes of learning and should be used following Studypool's honor code & terms of service.

This question has not been answered.

Create a free account to get help with this and any other question!

Related Tags

Brown University





1271 Tutors

California Institute of Technology




2131 Tutors

Carnegie Mellon University




982 Tutors

Columbia University





1256 Tutors

Dartmouth University





2113 Tutors

Emory University





2279 Tutors

Harvard University





599 Tutors

Massachusetts Institute of Technology



2319 Tutors

New York University





1645 Tutors

Notre Dam University





1911 Tutors

Oklahoma University





2122 Tutors

Pennsylvania State University





932 Tutors

Princeton University





1211 Tutors

Stanford University





983 Tutors

University of California





1282 Tutors

Oxford University





123 Tutors

Yale University





2325 Tutors