Organic Chemistry
Organic Chemistry
5th Edition
ISBN: 9780078021558
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Chapter 12, Problem 12.41P
Interpretation Introduction

Interpretation: The product formed when reaction only occurs on 2o alcohol of (R)-glycerolphosphate with NAD+ is to be predicted.

Concept introduction: The coenzyme nicotinamide adenine dinucleotide, NAD+ is used in biological systems for oxidation of alcohols to carbonyl compounds. In the oxidation of alcohols, NAD+ is reduced to NADH by the transfer of hydride from alcohols.

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JON Determine the bund energy for UCI (in kJ/mol Hcl) using me balanced chemical equation and bund energies listed? का (My (9) +36/2(g)-(((3(g) + 3(g) A Hryn = -330. KJ bond energy и-н 432 bond bond C-1413 C=C 839 N-H 391 C=O 1010 S-H 363 б-н 467 02 498 N-N 160 N=N 243 418 C-C 341 C-0 358 C=C C-C 339 N-Br 243 Br-Br C-Br 274 193 614 (-1 214||(=olin (02) 799 C=N 615 AAL
Determine the bond energy for HCI ( in kJ/mol HCI) using he balanced cremiculequecticnand bund energles listed? also c double bond to N is 615, read numbets carefully please!!!! Determine the bund energy for UCI (in kJ/mol cl) using me balanced chemical equation and bund energies listed? 51 (My (9) +312(g)-73(g) + 3(g) =-330. KJ спод bond energy Hryn H-H bond band 432 C-1 413 C=C 839 NH 391 C=O 1010 S-1 343 6-H 02 498 N-N 160 467 N=N C-C 341 CL- 243 418 339 N-Br 243 C-O 358 Br-Br C=C C-Br 274 193 614 (-1 216 (=olin (02) 799 C=N 618
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Chapter 12 Solutions

Organic Chemistry

Ch. 12 - Problem 12.11 (a) Draw the structure of a compound...Ch. 12 - Prob. 12.12PCh. 12 - Prob. 12.13PCh. 12 - Problem 12.14 Draw the products of each...Ch. 12 - Prob. 12.15PCh. 12 - Problem 12.16 Draw all stereoisomers formed when...Ch. 12 - Prob. 12.17PCh. 12 - Problem 12.18 Draw the products formed when both...Ch. 12 - Problem 12.19 Draw the products formed when each...Ch. 12 - Prob. 12.20PCh. 12 - Prob. 12.21PCh. 12 - Problem 12.22 Draw the products formed when each...Ch. 12 - Prob. 12.23PCh. 12 - Problem 12.24 Draw the organic products in each of...Ch. 12 - Prob. 12.25PCh. 12 - Prob. 12.26PCh. 12 - Problem 12.27 Draw the products of each Sharpless...Ch. 12 - Prob. 12.28PCh. 12 - 12.29 Draw the products formed when A is treated...Ch. 12 - Prob. 12.30PCh. 12 - 12.31 Devise a synthesis of the following compound...Ch. 12 - Prob. 12.32PCh. 12 - Prob. 12.33PCh. 12 - Prob. 12.34PCh. 12 - Prob. 12.35PCh. 12 - Prob. 12.36PCh. 12 - 12.37 Stearidonic acid (C18H28O2) is an...Ch. 12 - Draw the organic products formed when cyclopentene...Ch. 12 - Draw the organic products formed when allylic...Ch. 12 - Draw the organic products formed in each reaction....Ch. 12 - Prob. 12.41PCh. 12 - Prob. 12.42PCh. 12 - Prob. 12.43PCh. 12 - What alkene is needed to synthesize each 1,2-diol...Ch. 12 - Prob. 12.45PCh. 12 - 12.46 (a)What product is formed in Step [1] of the...Ch. 12 - Draw the products formed after Steps 1 and 2 in...Ch. 12 - 12.48 Draw the products formed in each oxidative...Ch. 12 - What alkene or alkyne yields each set of products...Ch. 12 - Prob. 12.50PCh. 12 - Prob. 12.51PCh. 12 - Prob. 12.52PCh. 12 - Prob. 12.53PCh. 12 - 12.54 An unknown compound A of molecular formula ...Ch. 12 - 12.55 DHA is a fatty acid derived from fish oil...Ch. 12 - Prob. 12.56PCh. 12 - 12.57 Draw the product of each asymmetric...Ch. 12 - 12.58 Epoxidation of the following allylic alcohol...Ch. 12 - Prob. 12.59PCh. 12 - 12.60 Identify A in the following reaction...Ch. 12 - Prob. 12.61PCh. 12 - 12.62 It is sometimes necessary to isomerize a cis...Ch. 12 - 12.63 Devise a synthesis of each compound from...Ch. 12 - Prob. 12.64PCh. 12 - Prob. 12.65PCh. 12 - 12.66 Devise a synthesis of each compound from the...Ch. 12 - Prob. 12.67PCh. 12 - Prob. 12.68PCh. 12 - 12.69 Devise a synthesis of each compound from as...Ch. 12 - Prob. 12.70PCh. 12 - Prob. 12.71PCh. 12 - 12.72 Draw a stepwise mechanism for the following...Ch. 12 - Prob. 12.73PCh. 12 - Prob. 12.74PCh. 12 - 12.75 Sharpless epoxidation of allylic alcohol X...
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