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Q: Which of the following molecules are nonpolar SO32-
A: ANSWER IS
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Q: which of the molecules is flat? a) C6H6 b) C6H12 (cyclohexane) c) CH4 d) CH2 = CH2 e) a and d
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Q: How many valence electrons should the following compound have (including bonds) SO3
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Q: what is the hybridization of secod carbon atom in butane?
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A: Detail description is given below to find out the structure of the compound
Q: How many sigma and hoe many pi bonds are there in one molecule of 3,3-dimethylpentane?
A: The structure for 3,3-dimethylpentane can be drawn as follows,
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Q: 1. What type of reaction that all organic compounds undergo?
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Q: which of the following compounds has only sigma bonds?
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- one of the chair structures of cis-1-chloro-3-methylcyclohexane is more stable than the other by 15.5 kj/mol (3.7kcal/mo) which is it ? what is the energy cost of a 1,3-diaxial interaction between a chlorine and a methyl group?Most naturally occurring amino acids have chiral centers (the asymmetric a carbon atoms)that are named (S) by the Cahn–Ingold–Prelog convention (Section 5-3). The commonnaturally occurring form of cysteine has a chiral center that is named (R), however.(a) What is the relationship between (R)-cysteine and (S)-alanine? Do they have the oppositethree-dimensional configuration (as the names might suggest) or the same configuration?(b) (S)-Alanine is an l-amino acid (Figure 24-2). Is (R)-cysteine a d-amino acid or anl-amino acid?Knowing that cyclohexane and hexene are isomers, suggest 2 methods allowing their separation.
- Iodide ion reacts with chloromethane to displace chlorideion in a common organic substitution reaction: I⁻+CH3Cl →CH3I+Cl⁻ (a) Draw a wedge-bond structure of chloroform and indicatethe most effective direction of Iattack.(b) The analogous reaction with 2-chlorobutane [FigureP16.107(b)] results in a major change in specific rotation asmeasured by polarimetry. Explain, showing a wedge-bondstructure of the product.(c) Under different conditions, 2-chlorobutane loses Clin arate-determining step to form a planar intermediate [FigureP16.107(c)]. This cationic species reacts with HI and then losesHto form a product that exhibits no optical activity. Explain,showing a wedge-bond structure.A 1,2-cis disubstituted cyclohexane, such as cis l,2-dichlorocyclohexane, musthave one group axial and one group equatorial. Explain.B + 2C ---> D + E
- Draw the skeletal (line-bond) structure for (5S), (3Z)-5-chlorohex-3-en-2-one. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Show proof for (5S) and (3Z).Two conformations of cis-l, 3-dimethylcyclobutane are shown. What is the difference between them, and which do you think is likely to be more stable?Rings + Unsaturation --- Hydrogenation If compound A C51H81BrN5O3P3 is hydrogenated to give compound B C51H101BrN5O3P3. How many rings does compound A have? Assume that P has a valency of 5. Would the answer be 4 rings? Formula -> unsat + rings = 1+C +N/2 - H/2 - X/2
- Kindly xplain the solubility of alkanes, alkenes, and alkynes to H2SO4.1.The [CoCl4]2- anion is intensely blue colored and [CoCl6]4- is a lightly colored pink. explain breifly 2.Why is the method of descending symmetry needed to derive an mo diagram for acetylene (ethyne), but not needed for diazene((NH)2)?One mole of an unknown hydrocarbon, compoundC,in the presence of a platinum catalyst, adds 98.9L of hydrogen, measured at 744mm Hg and 22°C, to form a saturated alkanewhich containsone ring. Whenone mole of compound Cis reacted with ozone,followed by reduction with (CH3)2S, four moles of only oneproductwasformed, whose condensed molecular formula is CHO-CHO. Give the structure ofcompound C. Explain your reasoning.