Functional Groups: MATCHING 1. sulfhydryl 2. carboxyl 3. carbonyl 4. phosphate 5. amino а.- ОН b. - NH2 c. C=0 d. – PO,2 е. — СООН f. – SH g. – CH3 6. hydroxyl 7. methyl Name an example of a macromolecule where you would find the functional groups specified above. For example, 1 above is sulfhydryl. What macromolecule would you find this within? Place the answer in 1. Then answer 2 for carboxyl, 3 for carbonyl, etc. 1. 3. 5. 6. 2. 4.

Functional Groups: MATCHING 1. sulfhydryl 2. carboxyl 3. carbonyl 4. phosphate 5. amino а.- ОН b. - NH2 c. C=0 d. – PO,2 е. — СООН f. – SH g. – CH3 6. hydroxyl 7. methyl Name an example of a macromolecule where you would find the functional groups specified above. For example, 1 above is sulfhydryl. What macromolecule would you find this within? Place the answer in 1. Then answer 2 for carboxyl, 3 for carbonyl, etc. 1. 3. 5. 6. 2. 4.

Biology (MindTap Course List)

11th Edition

ISBN:9781337392938

Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Publisher:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Chapter3: The Chemistry Of Life: Organic Compounds

Section: Chapter Questions

Problem 2TYU: VISUALIZE The structures depicted are (a) enantiomers (b) different views of the same molecule (c)...

See similar textbooks

Similar questions

Need help. Which one of the following statements is FALSE? Group of answer choices A.Beta-pleated sheets are part of the secondary structure of proteins B.The nitrogenous bases of DNA are located on the inside because they are hydrophobic in character C.The peptide bond is formed by dehydration synthesis D.Alpha helices are stabilized by attraction between the amino acid R groups E.The peptide bond is rigid and planar and has partial double bond character
Draw a peptide that includes Phenylalanine, Cysteine, Tyrosine and Tryptophan. Label them by name and abbreviation. Assume a pH of 7 when drawing the protonation state of ionizable chemical groups. Why do the aforementioned aminoacids absorb U-V light?
_______ groups are the acid part of amino acids and fatty acids. a. Hydroxyl (OH) b. Carboxyl (COOH) c. Methyl (CH3) d. Phosphate (PO4)
VISUALIZE The structures depicted are (a) enantiomers (b) different views of the same molecule (c) geometric (cistrans) isomers (d) both geometric isomers and enantiomers (e) structural isomers
PREDICT Do any of the amino acid side groups shown below have the potential to form an ionic bond with any of the other side groups shown? If so, which pair(s) could form such an association? (a)CH3 (b)CH2 COO (c)CH2 CH2 NH3+ (d)CH2 CH2 COO (e)CH2 OH
Which functional groups are present? Select all that apply -Carboxyl group-Amino group-Phosphate group-Methyl group-Hydroxyl group
Label each Amine (A–D) in Table 1 as primary, secondary, or tertiary. Which classes of amines – primary, secondary, or tertiary – can participate in hydrogen bonding with other identical molecules? Discuss as a team, and record your consensus. How many different combinations of hydrogen bonds are possible between the following two molecules? redraw the molecules, showing a hydrogen bond between them. Compare Amines A–D in Model 1. Discuss as a team, and explain why three of the amines have a higher boiling point than the alkane. One of the amines has the same boiling point as the alkane. Explain. Compare Amine (A) and Amine (B). Explain the difference in boiling point. Compare Amine (B) with amine (C). Explain the difference in boiling point. Compare Amine (C) with amine (D). Explain the difference in boiling point. Compare Amine (D) with the alcohol. Work as a team to explain the difference in boiling point. Compare the amide with the alcohol. Explain the difference in boiling point.…
Modify isoleucine to show the predominant forms at pH 1, 7, and 13. Isoleucine has p?ap�a values of 2.4 (carboxyl group) and 9.7 (amino group).
The surface of the eye is wet by tears, and to minimize evaporation, the tear layer is coated with lipids. One of these lipids is built from oleic acid and a 32-carbon fatty acid that has a double bond between carbons 9 and 10 and a hydroxyl group attached to the omega carbon. The carboxyl group of oleic acid condenses with the hydroxyl group in the longer lipid. Draw the structure of the reaction product. It’s OK to draw a condensed structure.
Peptide bond formation occurs between which functional groups? SELECT ALL THAT APPLY A. Amino B. Carboxyl C. Alpha-Carbon D. Nitrogen
Differences between Cis-fatty acid VS. Trans fatty acids Limit your answer to two sentences only to every question. Copy and complete the table. GIVEN: DRAW THE EXPANDED STRUCTURE NAME THE BONDS [Molecular Orbitals &Hybrid Orbitals] IUPAC NAME CHOOSE THE SIMPLEST Unsaturated FATTY ACID NAME OF THE COMPOUND Cis-fatty acid Trans-fatty acid
using the expanded structure of Levothyroxine. Determine the molecular geometry of each central atom. Color each central atom based on its molecular geometry and include a key for your colors. For example, color tetrahedral C’s red, trigonal planar C’s , blue, etc.