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- Answer the following: (i) Haloalkanes easily dissolve in organic solvents, why? .. (ii) What is known as a racemic mixture ? Give an example. (iii) Of the two bromoderivatives, C6H5CH(CH3)Br and C6H5CH(C6H5)Br which one is more reactive in SN1 substitution reaction and why?Propose a reason(s) for tertiary alcohols being unreactive with most oxidizing agents.Draw structures corresponding to the following names: (a) 3, 3-Dimethyl-4-octyne (b) 3-Ethyl-5-methyl-1, 6, 8-decatriyne (c) 2, 2, 5, 5-Tetramethyl-3-hexyne (d) 3, 4-Dimethylcyclodecyne (e) 3, 5-Heptadien-1-yne (f) 3-Chloro-4, 4-dimethyl-1-nonen-6-yne (g) 3-sec-Butyl-1-heptyne (h) 5-tert-Buty1-2-methyl-3-octyne
- Axial alcohols are oxidized faster than equatorial alcohols by PCC andother Cr6+ oxidants. Which OH group in each compound is oxidizedfaster?hi! i need answers on letters d to f. The instructions says give the IUPAC name of each compound. Thank u!Choose from the given choices: A. alkanes B. carboxylic acids C. amines D. phenols E. alkyl halides F. ketones G. aldehydes H. alcohols Will dissolve in water and will dissolve also in sodium bicarbonate with the release of carbon dioxide as biproduct. Will not dissolve in water but will dissolve on both strong base and sodium bicarbonate and no liberation of carbon dioxide 3-4. .Will not dissolve in water and on strong acids and bases. 5. Will dissolve in water and will change the blue litmus into red
- HURRY ASAP I WILL RATE NO NEED FOR EXPLANATION WHICH OPTIN Which of the following statement(s) about the alcohols of which their structures/IUPAC names are given below is/are true? I. CH3-CH(OH)-CH2-CH2-CH(CH3)-CH2-CH3 II. CH3-CH(OH)-CH2-CH2-CH2-CH3 III. Cyclohexanol IV. (CH3)2-C(OH)-CH2-CH2-CH3 V. CH3-CH2-OH The IUPAC name of compound I is 3-methyl-6-heptanol. Compound V is a secondary alcohol Compound III is primary alcohol. Compound IV is tertiary alcohol Compounds I and II are primary alcoholsUsing molecular models as well as structural drawings, explain why trans-decalin is rigid and cannot ring-flip whereas cis-decalin can easily ring-flip.What is the structure ,melting point,boiling point ,molecular weight and molecular formula for 2,4 dinitrochlorobenzen, 2,4 dinitrophenylaniline and 2,4 dinitrochloroaniline thank u just want these i just put a blank pic coz it doesnt submit
- #B: Methyl acetate has methoxy, -OCH3 as the remaining of the alcohol part in the ester. Isopropyl acetate has isopropoxy, -OCH(CH3)2 as the remaining of the alcohol part in the ester. -OCH(CH3)2 is more electron donating than the methoxy, -OCH3 group due to the presence of two electron-donating -CH3 group in the former. Hence saponification reaction of Isopropyl acetate is much slower than methyl acetate. Hence the rate of saponification of methyl acetate, CH3CCO2CH3 is 50 times greater than that for isopropyl acetate.Draw 2‑methylpropanal. Include all hydrogen atoms. Predict the products when cyclohexanol is heated in the presence of H+.H+. Show all hydrogen atoms.wt of flask = 98.4669 wt of product = 20.7868 wt of flask and product = 119.2537 weight of water collected = 4.4 mL wt of water expected 4.5 mL percent yeild of ester = 71.58% 19.0 mL of 0.25 M n-propanol 18.5 mL propionic acid plz answer questions below