Question

A) Draw the structure of aspirin. Circle and identify three functional groups in the molecule. b)...

A) Draw the structure of aspirin. Circle and identify three functional groups in the molecule.

b) can one get relief from expired aspirin? Why or why not?

c) buffering is aspirin mixed with magnesium carbonate. What is the purpose of magnesium carbonate in the formation?

Homework Answers

Answer #1

b)

It smells like vinegar because it has decomposed into salicylic acid and acetic acid. Acetic acid is essentially vinegar. It will still work as an analgesic (pain reliever) but it will no longer have an effect on platelet aggregation - blood clotting. Aspirin will normally (when not expired) help "thin" the blood - an important role when someone is having a heart attack. If you give someone an expired aspirin that is having a heart attack, it will not help to save thier life. Also, since the tablet is now more acidic from decomposition, it can (and most likely will) cause stomach upset.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
A) Label the functional groups present in aspirin and acetaminophen (except the benzene ring). Would you...
A) Label the functional groups present in aspirin and acetaminophen (except the benzene ring). Would you consider these compounds nonpolar, moderately polar or very polar? Circle the most acidic hydrogen in each structure. B) Draw the corresponding salt for Aspirin (when extracted with aqueous NaHCO3)
Column Chromotography Lab: Draw structure of acetylferrocene (circle functional groups). Why does acetylferrocene remain on the...
Column Chromotography Lab: Draw structure of acetylferrocene (circle functional groups). Why does acetylferrocene remain on the column when you elute with the hexane solvent and then why does it come off the column with the second solvent, CH2Cl2/EtOAc?
A)Draw the three most important contributing structures for the molecule with the formula c4h4o which has...
A)Draw the three most important contributing structures for the molecule with the formula c4h4o which has no OH bond and one ring of four carbons. Be sure to show all valence shell lone pairs and all charges B) what is the strongest bond in the molecule in the most important contributing structure C) what is the total number of this molecule that lie in the same plane D) what is the ideal HCH bond angle in this molecule E)Predict whether...
[A] List all the structural features (chains, rings, functional groups, # of C's, rings, etc) the...
[A] List all the structural features (chains, rings, functional groups, # of C's, rings, etc) the compound 5-Chloro-3-(2,2-DiChlorobutyl)CycloPentene has. (Or, tell what each part of the compound's name is telling us, i.e. what: (1) Di, (2) Chloro, (2) Butyl, (3) Cyclo, (4) Pent, (5) Ene mean and (6) why the ()'s after the 3 are used?) [B] In the name, what do the numbers: 2's, 3 & 5 tell us? [C] Why don't we need a number to indicate where...
1. Draw the line-bond structure for stearic acid and linoleic acid. Identify which fatty acid is...
1. Draw the line-bond structure for stearic acid and linoleic acid. Identify which fatty acid is saturated and which is unsaturated. 2. Trans fats are produced during the hydrogenation of polyunsaturated oils.             a. What is the typical configuration (cis or trans) about the double bond of a monounsaturated fatty acid? b. Draw the structure of cis-palmitoleic acid. c. Draw the structure of trans-palmitoleic acid. d. Why are trans-fatty acids considered to be a health hazard? e. Is it better...
1. HF boils at 20 °C, and methanol (CH3OH) boils at 65 °C.   In which molecule...
1. HF boils at 20 °C, and methanol (CH3OH) boils at 65 °C.   In which molecule do you expect the hydrogen bonding interactions to be stronger? Why? (2 points) In which molecule do you expect the (non-hydrogen bonding) dipole-dipole interactions to be stronger? Why? Draw both molecules and sketch the direction of the dipole moment. (4 points) In which molecule do you expect the London dispersion forces to be stronger? Why? (3 points) Based on the boiling points given above,...
Tetrafluoroethylene (C2F4) is the molecule from which teflon is made. Draw the Lewis Structure for C2F4...
Tetrafluoroethylene (C2F4) is the molecule from which teflon is made. Draw the Lewis Structure for C2F4 Does C2F4 contain polar or nonpolar bonds? Is C2F4 Polar or Nonpolar? State the hybridizations of the two C atoms in C2F4 Give the electron geometries of the two C atoms in C2F4 Give the bond angles in C2F4 Teflon is formed when C2F2 is polymerized, or in other words, when the pi bonding electrons are used to form sigma bonds between molecules, linking...
A)Draw a Lewis structure for BCl3 (remember that B is a frequent exception to the octet...
A)Draw a Lewis structure for BCl3 (remember that B is a frequent exception to the octet rule). Part B Determine molecular geometry of BCl3. A)linear B)bent C)trigonal planar D)trigonal pyramidal Part C What kind of intermolecular forces are present in BCl3? (Can be more then one) A) dispersion force B) dipole-dipole force C) hydrogen bond Part D Draw a Lewis structure for HCOH (carbon is central; each H and O bonded directly to C) Part E Determine molecular geometry of...
For the following amino acid strand (shown from N to C-terminus) Asp-Pro-Cys-Gly-Ser-Try A.) Draw the structure...
For the following amino acid strand (shown from N to C-terminus) Asp-Pro-Cys-Gly-Ser-Try A.) Draw the structure of the hexapeptide w/ appropriate stereochemistry.    B.) What forces hold the above peptide in an α-helix? What part of the peptide is involved? C.) This hexapeptide is one of three peptide chains in a protein. What forces hold the above peptide in its 4o structure?
3. Imagine three treatment groups are being compared using Analysis of Variance. What effect would each...
3. Imagine three treatment groups are being compared using Analysis of Variance. What effect would each of the following have on an F score (make it smaller, make it larger, or cause no change)? Explain why. a. A large within-group error. b. One group with a mean that is two standard deviations away from the other groups. c. A great deal of overlap between two groups. d. Adding a bunch of outliers (extreme scores) to all three groups being compared.