Give one possibility for the mystery reactant R in this organic reaction:NiR + H2CH3-CH2-CH3Specifically, in the drawing area below draw the condensed structure of what R might be. There may be more than one correct answer.Note: keep in mind that the equation above states R and H2 are present in a 1:1 mole ratio.

Approach to solving the question:Rational Detailed explanation:An organic reaction is a chemical…

Answered: Give one possibility for the mystery…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL2: Mass Spectrometry

Section: Chapter Questions

Problem 20CTQ

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The chemical structure of propane (C3H3) is provided below. Which of the following isomers is propane able to form? Briefly justify your answer (2- 3 sentences) A. Structural isomer B. Cis-trans isomer C. Enantiomer D. All of the above E. None of the above н ннн H-C-C-C-H H. ннн H.
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Below, write the names of 7 organic compounds whose open structures are given, and the open structures of 8 organic compounds that have been named according to the IUPAC naming system. (Consider also the case of R, S or E, Z.
I. Molecule's Degree of Unsaturation* *to avoid confusion, we shall use "degree of unsaturation" to refer to the number of pi bonds or number of rings present in the molecule as a result of the loss of hydrogen atoms when referenced using the alkane formula of C,„H2n+2" The numerical value for the degree of unsaturation = 1 means that a molecule of hydrogen, H,, or two atoms of hydrogen are lost and instead 1 pi bond OR 1 ring is seen in the molecule. For this exercise, determine the degree of unsaturation of each of the following compounds: CH3 1. 2,3,3-Trimethyl-1,4,6-octatriene CH3 6. CH3 2. 3-Ethyl-2,2,-dimethyl-3-heptene `CH3 3. 2-Methyl-1,5-hexadiene 8. 7. ÇH3 H. CH3 4. 4-tert-Butyl-2-methylheptane Answers: 1. L2. 3. _4. 5. 6. _7. 8. 5.
(c) There is one (1) other positional isomer of X missing for reaction II. Draw the structural formula of this isomer.
Answer this question:How to draw the line bond formula or lewis structure of a methyl ketone with the chemical formula C6H5C3H5O? (also taking into consideration the solubility test and chemical test results provided below) Based on the results of the solubility tests the compound is insoluble in water, 10% NaOH and 10% HCl but soluble in concentrated H2SO4. The functional group/class is identified to be Methyl Ketone, based on the results of the chemical tests on Table 2. CHEMICAL TEST OBSERVATIONS +(compound tested positive for the chemical reaction)/ otherwise (-) Molisch test turbid colorless solution - 2,4-DNP test formation of orange-yellow precipitates + Tollen’s test turbid colorless solution - Ninhydrin test clear pale-yellow solution - iodoform test clear pale-yellow solution +
I need help with number 16
naming a chemical compound. I'm currently learning how to name alkanes and alkyl halides. Im confused about the compound ethanal, or acetaldehyde. The second carbon has a double bond on its hydrogen, so I'm wondering why the infix is "an" instead of "en". Frpm the table of infixes, it says "an" is for single bonds. Can someone help me understand
From what we know today, what do the two Kekulé structures for benzene really represent? August Kekulé was the first person to propose a viable structure for benzene in 1865. Structures that can be separated at low enough temperatures (near absolute zero). Structures that are in a state of rapid equilibrium. O Structures that are in resonance. Structures that are conjugated trienes (--C=C--C%3DC--C3C--).
Fatty acids are molecules with a carboxylic acid on one end and long hydrocarbon chain on the other. The sodium salts of fatty acids (such as sodium strearate, shown below) are commonly used in soaps to trap nonpolar dirt and grease particles. Soap does not work well in "hard water, which is water with high concentration of magensium and calcium ions (often found in water obtained from wells) Explain this observation at a molecular level.
Chemistry 2.) Draw the condensed structures (NOT line structures) for the following reactions of alcohols. CH3 a.) H3C- [H'] CH2-CH- CH3 CH3 H3C-CH-CH3 b.) H;C-CH2-CH-CH2 CH2-OH [0]
An oxidation reaction is done on a) 1-hexanol, b) 2-hexanol, c) 3-hexanol, and d) 2- methyl-2-pentanol. Using skeletal structures, draw the END product for each reaction a-d. Use () to surround functional groups and write after the carbon it is bonded, use the equal sign for a double bond. If there is no reaction, type No RXN.

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