(a)
Interpretation:
Structural formula for 2,2-dibromobutane has to be drawn.
Concept Introduction:
Organic compounds can be drawn from its IUPAC name. Initially, the parent chain is identified from the IUPAC name. After that the carbon chain is drawn with carbon atoms alone. Next step is to add the substituents in the respective positions as indicated in the IUPAC name. Remaining valency of carbon atom is satisfied by adding correct number of hydrogen atoms.
Structural formula is the representation of the organic compound by showing all the bonds that is present between the atoms. Even though complete structural information can be obtained using the structural formula, it consumes too much space and time for drawing large molecules.
(b)
Interpretation:
Structural formula for 2-iododecane has to be drawn.
Concept Introduction:
Refer part (a).
(c)
Interpretation:
Structural formula for 1,2-dichloropentane has to be drawn.
Concept Introduction:
Refer part (a).
(d)
Interpretation:
Structural formula for 1-bromo-2-methylpentane has to be drawn.
Concept Introduction:
Refer part (a).
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Chapter 10 Solutions
GENERAL, ORGANIC, BIOCHEM (LL W/ ACCESS)
- Don't used hand raiting and don't used Ai solutionarrow_forward13.84. Chlorine atoms react with methane, forming HCI and CH3. The rate constant for the reaction is 6.0 × 107 M¹ s¹ at 298 K. When the experiment was run at three other temperatures, the following data were collected: T (K) k (M-1 s-1) 303 6.5 × 107 308 7.0 × 107 313 7.5 x 107 a. Calculate the values of the activation energy and the frequency factor for the reaction. b. What is the value of the rate constant in the lower stratosphere, where T = 218 K?arrow_forwardMy Organic Chemistry textbook says about the formation of cyclic hemiacetals, "Such intramolecular reactions to form five- and six-membered rings are faster than the corresponding intermolecular reactions. The two reacting functional groups, in this case OH and C=O, are held in close proximity, increasing the probability of reaction."According to the book, the formation of cyclic hemiacetals occurs in acidic conditions. So my question is whether the carbonyl group in this reaction reacts first with the end alcohol on the same molecule or with the ethylene glycol. And, given the explanation in the book, if it reacts first with ethylene glycol before its own end alcohol, why would it? I don't need to know the final answer. I need to know WHY it would not undergo an intermolecular reaction prior to reacting with the ethylene glycol if that is the case. Please do not use an AI answer.arrow_forward
- Don't used hand raiting and don't used Ai solutionarrow_forwardHighlight in red each acidic location on the organic molecule at left. Highlight in blue each basic location on the organic molecule at right. Note for advanced students: we mean acidic or basic in the Brønsted-Lowry sense only. Cl N شیخ x Garrow_forwardQ4: Draw the mirror image of the following molecules. Are the molecules chiral? C/ F LL CI CH3 CI CH3 0 CI CH3 CI CH3 CH3arrow_forward
- Complete combustion of a 0.6250 g sample of the unknown crystal with excess O2 produced 1.8546 g of CO2 and 0.5243 g of H2O. A separate analysis of a 0.8500 g sample of the blue crystal was found to produce 0.0465 g NH3. The molar mass of the substance was found to be about 310 g/mol. What is the molecular formula of the unknown crystal?arrow_forward4. C6H100 5 I peak 3 2 PPM Integration values: 1.79ppm (2), 4.43ppm (1.33) Ipeakarrow_forwardNonearrow_forward
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