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- (1R)-1-chloro-1-cyclohexylpropan-1-ol Draw the bond-line structure of the said compoundBromine is a larger atom than chlorine, but the equilibrium constants in Table 3.9 indicate that a chloro substituent has a greater preference for the equatorial position than does a bromo substituent. Suggest an explanation for this fact.Draw a structural formula for the most stable carbocation with each molecular formula. Q.) C3H7O+
- Using the table of average bond dissociation enthalpies at 25°C, determine which of the following reactions are energetically favorable at room temperature. Assume that ▲S = 0. Q. CH2=CH2 + (CH3)3SiH --> CH3CH2Si(CH3)3Which of the following molecules has only single bonds. A. CHCHCH3 B. CH2CHCH3 C. CH3CH2CCH D. CH3CH3 E. CH2CH2 Which of the following molecules has a carbon-to-carbon double bond? A. CH3CCH B. CHCH C. CH3CH3 D. CH3CH2CH3 E. CH2CHCH3Use bond-dissociation enthalpies to calculate the AH° for each of the following reactions. CH3CH2CH3+H2 → CH3CH3+CH4 CH3CH2CL+HI → CH3CH2I+HCI
- 1. Write bond-line formulas for (a.) four aldehydes with the formula of C5H10O (b) three ketones that have the formula C5H10O (c.) four carboxylic acids with the formula C5H10O2 (d.) three esters with the formula C5H10O23. Classify the alcohols shown below as primary, secondary, or tertiary. A) secondary B) primary C) tertiary 1) CH3 - CH2 - OH 2) CH3 | CH3 - C - CH2 - OH | CH3 3) OH | CH3 - CH - CH3 4) 5) CH3 | CH3 - C - CH2 - CH3 | OH 4. Identify the product, if any, that would form in each of the following reactions. A) CH3 - CH3 B) CH3 - CH2 - CH3 C) OH | CH3 - C H - CH3 D) O CH3 - C - OH E) CH3 - CH2 - OH 1) O CH3 – C - H 2) O CH3 - C - CH3 + H2 3) O CH3 - C - H + H2Which of the following can form H-bonds? a) AsH3 b) HBr c) CH3CH2CH3 d) CH3OH e) CH3OCH3