### Structural Formulas of Organic CompoundsThe image illustrates several structural formulas of organic compounds, showcasing different arrangements of atoms and bonds. Each structure will be described below in detail:#### Structure 7:- Formula: ``` H H O | | || H — C — C — C — OH | | H H ```- Description: This is a linear chain of three carbon atoms. The first carbon (leftmost) is bonded to three hydrogen atoms. The second carbon is bonded to two hydrogen atoms and a carbonyl group (C=O). The third carbon is bonded to one hydrogen atom and a hydroxyl group (OH).#### Structure 8:- Formula: ``` H O | || H — C — C — O — H | H ```- Description: This structure shows an ethanol molecule with an additional oxygen and hydrogen in a functional group. One carbon is singly bonded to three hydrogens and a second carbon. The second carbon is doubly bonded to oxygen (carbonyl group) and has a single bond with oxygen, which is further bonded to a hydrogen atom.#### Structure 9:- Formula: ``` H H | | H — C — C — O — H | | H H ```- Description: This structure shows an ethoxyethane with each carbon double-bonded to an oxygen atom and single-bonded to three hydrogens on each side.#### Structure 10:- Formula: ``` H H O | | || H — C — C — C — OH | | | H H H ```- Description: This structure illustrates propanol. The first carbon is bonded to three hydrogen atoms and a second carbon. The second carbon is bonded to two hydrogen atoms and a third carbon. The third carbon is bonded to one hydrogen atom and a hydroxyl group (OH).#### Structure 11:- Formula: ``` H H | | | H — C = C — H | | H H ```- Description: This represents an ethylene molecule (ethene) where two carbon atoms are double-bonded to each other, with **Naming Organic Compounds**Use your notes and the Tables P, Q, and R in your Reference Guide to name each of the following organic compounds.

The naming of the organic compound is based on the functional group present in that organic…

Answered: μαζ Η Η H-C-C-30 ΦΗ Η Η Η Η Η H-c-9-9-c…

μαζ Η Η H-C-C-30 ΦΗ Η Η Η Η Η H-c-9-9-c Η Η Η το Он 8. 11 Η Ο .. H_c-c-o-H . H H 0 H H-C-C-C-H 1 Η Η 12. Η Η Τι H-C-C-0 H H H H ... B-C-C-C-H H OH H

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Step 3 of 8 Sum the equations for d[H] and d[Br] and solve for [Br]. (Use the following as necessary: [Br2], [H], [H2], [HBr], k1, k2, k3, k4, and k5.) dt dt [Br] = K5 2k1 [Br.] 2k [Br2] ks Step 4 of 8 Using the equation for I from Step 2, solve for [H]. (Use the following as necessary: [Br], [Br2], [H2], [HBr], k1, k2, k3, k4, and k5.) dt ky[ Br][H,] kg[Br] + k4 [HBr] [H] = k2[Br][H2] k3[Br2] + k4[HBr] Step 5 of 8 Substitute the equation for [Br] from Step 3 into the equation for [H] from Step 4 and simplify. (Use the following as necessary: [Br2], [H2], k1, k2, k3, k4, and k5.) k, k5 [Br.] [H] k3[Br2] + k4[HBr] Submit
9. Determine whether the following drugs comply with Lipinski's rule. Also investigate the "alternative criteria" (rotatable bonds, polar surface area) for both drugs. OH N(CH3)2 HO. OH OH OH O Tetracycline (antibiotic) P=0.04 OH CONH₂ OH N. Naloxone (morphine agonist) P=83
Give detailed Solution with explanation needed of all..don't give Handwritten answer - H HHHHH - C-H | | H I | H | HH | C-H - C | | H | - H | | H ☐ | H H HHHHHHH H C - - C. - H H H | C structure - H | H H | C | - C | - C - | C H - ☐ H name Name these organic compounds:
HO Но MO!!!! OH Но не MeDH (excess) 1
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Naming Organic Compounds Use your notes and the Tables P, Q, and R in your Reference Guide to name each of the following organic compounds.
2 NO₂(g) → N₂ O₁ (g) O 2511041 O > 0 O ▲,$, O A.S. Q Search 9999 100 # on D KELIAV G 24 G
||| O NAMING AND DRAWING ORGANIC MOLECULES Naming normal alkanes Name these organic compounds: 43°F Mostly sunny Explanation structure H I H-C-H H H H H H H H 1 | | | | | | | -C. C-C H-C-C. | | H H Check | 1 I H H H | С-Н | H H н-с | H H H 1 -C-H X Q Search name Ś [***] 0/3 a Jessica V ? 0 000 B © 2023 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility 8:50 PM 4/23/2023 نشاء +
2A + b <-> C. Kc = 9.1C + D <-> 2E. Kc = 3.2 calculate Kc for: A + 1/2B + 1/2D <-> E
MyCSU-Columbus State Univers X M Inbox (1) - bailes_amber@colum X D2L Quiz 1- Intro Resrch Meth in CJ K ← → CO 03 Email MGmail X A ALEKS-Amber Bailes - Learn X + www-awu.aleks.com/alekscgi/x/Isl.exe/1o_u-IgNslkr7j8P3jH-IJgXZp57itWHhRgilODc5MqvhZbKYx2-U-03700TYd4ABbH6KAJLiK5JfbHdk1X12WQ... LE YouTube Maps MyCSU-Columbus... B Homepage - Georg... Microsoft Office Ho... BLesson 2 Discussion... III MyMidland Mortga... CHEMICAL REACTIONS Solving for a reactant using a chemical equation 3/5 Green plants use light from the Sun to drive photosynthesis. Photosynthesis is a chemical reaction in which water (H₂O) and carbon dioxide (CO₂) chemically react to form the simple sugar glucose (C6H₁2O6) and oxygen gas (0₂). 12 What mass of carbon dioxide is consumed by the reaction of 3.6 g of water? Be sure your answer has the correct number of significant digits. g x10 Ś ? Explanation Ⓒ2022 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Ce 78°F O Et C ||| Check Type here to search X a no…
H H ÇH2OH ÇH2OH HOʻHÓ H-C-OH H-C-OH НО—С—Н C=0 C=0 C=0 H-C-OH H-C-OH HO-C-H H-C-OH H-C-OH H-C-OH H-C-OH LoH H-C-OH H-C-OH H--OH H-C-OH H-C-OH CH,OH H-C-OH ČH2OH ČH,OH ČH,OH ČH,OH 1 2 4 Wh of the sugars can form pyranoses without undergoing isomerization to a different sugar? Select one or more: а. 2 b. 3 С. 5 е. 4 d.