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Q: eq [References] Write IUPAC names for the compounds below. If you use them, abbreviate ortho-, meta-…
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Q: 3. Name the following compound. CH3 CH-CH3 H.
A: 1. The IUPAC name of the above compound is 4,4-dimethylheptane.
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Q: C. d. e. CH3. H CH2-CH3 (use cis/trans prefix when naming) ОН OH C Br Н
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Q: (1) (2) (3) CH,=CH CH,-0-CH,-CH=CH,
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Q: structure name CH; CH,- C= CH– CH, CH, сH, — сн, — с — сн, CH3 CH;- CH – C= CH
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Q: Give the major organic product H20 CH; CH;CH,C=CH HgSO, H;SO.
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Q: Complete the following reaction by writing the name of the product. Ni or Pt CH;CH,CHC-H H2 CH,CH,
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Q: 1. Give the IUPAс пате of the following compounds: (al DI HyC=CHCHCCH, CHyCH;CH- CH,CH, (c) (d)…
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Q: 5. Give the IUPAC name of the following carboxylic compounds. а. СН,CH,CEССООН b.…
A: Please find the below attachments.
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Q: 2. Give IUPAC names to the following compounds. A. CO2H iHH NH2 В. CN ČO,H С. OH
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Q: * Deter miine the missing compound, and give their IUPAC name. AVD CHス-C三C-CHz-CHz-CH3+ 2H2 Po, pd,…
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Q: Select one: а. (CH2OH)2 o b. CH4 с. СН3ОН
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- Is the reaction of 1-butene with HBr regioselective? a. Is it stereoselective? b. Is it stereospecific(a) Why does p-dichlorobenzene have a higher m.p. than its o- and m-isomers?(b) Why is (±)-Butan-2-ol optically inactive?cis-1,2-Dimethylcyclohexane is optically inactive even though it has two chirality centers. Explain.
- Rank the following groups in order of decreasing priority. a. – COOH, – H, – NH2, – OH b. – H, – CH3, – Cl, – CH2CI c. -CH2CH3, -CH3, -H, -CH(CH3)2 d. – CH = CH2, – CH3, – C ≡ CH, – HRank the following groups in order of decreasing priority. −C≡CH, −CH(CH3)2, −CH2CH3, −CH=CH2Draw the structural formula for at least one bromoalkene with the molecular formula C5H9Br that shows: Q.) Neither E,Z isomerism nor chirality
- Draw two diasteriomers of (1Z,4R)-1,4-dimethylcyclodecene and give the IUPAC name including E/Z and R/S notation.a. Draw the structures and give the common and systematic names for alkynes with molecular formula C7H12. Ignore stereosiomers. (Hint: There are 14.) b. How many would there be if stereoisomers are included?Rank the following groups in order of decreasing priority. −H, −CH3, −Cl, −CH2Cl
- 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/2Draw (2R, 3S)-diaminopentaneIf I chlorinate 2-bromo-1-chloropropane under light, how many products do I obtain? Are any chiral?