Concept explainers
(a)
Interpretation:
For each
Concept introduction:
The small molecular units from which
(b)
Interpretation:
For each nucleotide, it is to be stated whether it can be part of RNA or DNA.
Concept introduction:
In both RNA and DNA, the backbone of a single strand consists of alternating sugar and phosphate group. In RNA, the sugar group is ribose whereas in DNA, it is deoxyribose. In the ribose sugar, the
(c)
Interpretation:
The nitrogenous base in each of the given nucleotides is to be identified.
Concept introduction:
Nucleotides are distinguished from one another by identifying the nitrogenous bases attached to the sugar group. In both RNA and DNA, it is the specific sequence of the nitrogenous bases that determines the genetic information that is stored or carried. There are four types of five nitrogenous bases that could be present in RNA and DNA. Uracil, guanine, adenine, cytosine, thymine are the nitrogenous bases present in RNA and DNA. In a nucleotide, the
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ORGANIC CHEMISTRY:PRINCIPLES...(PB)
- Sketch either the expanded or condensed structure for the following molecule: 7-methyl-4-octyne Then choose the correct option that applies to each feature of its structure. How many carbons are in the parent chain? ["", "", "", "", "", "", "", ""] Is there a double bond? ["", ""] Is there a triple bond? ["", ""] At what carbon number is the multiple bond? Choose 0 if no multiple bond is present. ["", "", "", "", "", "", "", "", "", "", ""] How many H are attached to carbon 7?arrow_forwardDoxorubicin, shown here, is an important chemotherapy drug used to treat avariety of cancers, including bladder cancer, breast cancer, and certain forms of leukemia. Doxorubicin works by binding to DNA in such a way that a portion of it penetrates the DNA double helix— a process called intercalation. During transcription— the process that forms RNA— portions of the DNA strands are temporarily separated for the base sequence to be read and then are reconnected. With bound doxorubicin, however, the double helix does not reform properly after the strands are separated, which disrupts replication— the process that forms an identical copy of DNA. Which portion of doxorubicin do you think intercalates into the DNA double helix, and why do you think it has little difficulty doing so?arrow_forwardProblem (#2.) For each ion below, draw all reasonable resonance structures (linked by resonance arrows “↔”). Include curved arrows that indicate the movement of electrons between each resonance structure. Assign non-zero formal charges to each atom for each resonance structure. (a.) NO3– (nitrate) (b.) CH3COO– (acetate) (c.) N3– (azide) (d.) NCO– (isocyanate) Problem (#3.) For each ion in question 2, draw a resonance hybrid, assigning non-zero formal and/or partial charges (δ+, δ–) as needed. Problem (#4.) For each skeletal structure below, satisfy the valences (or octets) of all of the atoms by filling in double and triple bonds as well as unshared electron pairs. Assign non-zero formal charges and show the overall charge if the structure is an ion. See photo attached for Problem number 4. Problem (#5.) For each structure in question 4, draw a resonance hybrid (if it has one) and assign non-zero formal and/or partial charges as needed.arrow_forward
- Please answer a) and b)arrow_forwardE. Sketch an example of a hydrophobic interaction (hydrophobic pocket) that could be ound in a protein.arrow_forwardTextbook Problem Which of the terms glycerophospholipid, sphingophospholipid, and sphingoglycolipid applies to each of the following characterizations? More than one term may apply, or none of the terms may apply in a given situation a. Membrane lipid b. Saponifiable lipid c. Amide linkage present d. Has a "head and two tails" structurearrow_forward
- For the following Structure, a) draw in any missing lone pairs; b) identify and list the resonance patterns (i.e. allylic cation) present. If one pattern shows up more than once, list it multiple times c) draw curved arrows on the initial structure to produce a resonance structure, including formal charge. (hint - use a minimum of curved arrows for each resonance structure). Repeat on the second structure to generate a third structure. Rank the resonance structures in order of decreasing importance: 1 is most important, 2 is second most important, etc... H Pattern 1: Pattern 2: Rank: Pattern 1: Pattern 2: Rank: Pattern 1: Pattern 2: Rank:arrow_forwardI struggle all of them on table because I don't understand this question. Could you help me, pleasearrow_forward3arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning