ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
6th Edition
ISBN: 9781319306977
Author: LOUDON
Publisher: INTER MAC
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Question
Chapter 4, Problem 4.6P
Interpretation Introduction
(a)
Interpretation:
The structure of the given compound is to be drawn.
Concept introduction:
The systematic naming of organic compound is given by
Rules for writing structural formula from IUPAC name are:
- First identify the longest carbon chain.
- The next step is to identify the
functional groups present in the compound. - Identify the position, location, and number of the substituent bonded to the carbon chain.
Interpretation Introduction
(b)
Interpretation:
The structure of the given compound is to be drawn.
Concept introduction:
The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.
Rules for writing structural formula from IUPAC name are:
- First identify the longest carbon chain.
- The next step is to identify the functional groups present in the compound.
- Identify the position, location, and number of the substituent bonded to the carbon chain.
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Please note that it is correct and explains it rightly:The proportion of O, C and H in the graphite oxide is:a) Constant, for the quantities of functional groups of acids, phenols, epoxy, etc. its constantsb) Depending on the preparation method, as much oxidant as the graphite is destroyed and it has less oxygenc) Depends on the structure of the graphic being processed, whether it can be more three-dimensional or with larger crystals, or with smaller crystals and more borders.
Chapter 4 Solutions
ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
Ch. 4 - Prob. 4.1PCh. 4 - Prob. 4.2PCh. 4 - Prob. 4.3PCh. 4 - Prob. 4.4PCh. 4 - Prob. 4.5PCh. 4 - Prob. 4.6PCh. 4 - Prob. 4.7PCh. 4 - Prob. 4.8PCh. 4 - Prob. 4.9PCh. 4 - Prob. 4.10P
Ch. 4 - Prob. 4.11PCh. 4 - Prob. 4.12PCh. 4 - Prob. 4.13PCh. 4 - Prob. 4.14PCh. 4 - Prob. 4.15PCh. 4 - Prob. 4.16PCh. 4 - Prob. 4.17PCh. 4 - Prob. 4.18PCh. 4 - Prob. 4.19PCh. 4 - Prob. 4.20PCh. 4 - Prob. 4.21PCh. 4 - Prob. 4.22PCh. 4 - Prob. 4.23PCh. 4 - Prob. 4.24PCh. 4 - Prob. 4.25PCh. 4 - Prob. 4.26PCh. 4 - Prob. 4.27PCh. 4 - Prob. 4.28PCh. 4 - Prob. 4.29PCh. 4 - Prob. 4.30PCh. 4 - Prob. 4.31PCh. 4 - Prob. 4.32PCh. 4 - Prob. 4.33PCh. 4 - Prob. 4.34PCh. 4 - Prob. 4.35PCh. 4 - Prob. 4.36PCh. 4 - Prob. 4.37PCh. 4 - Prob. 4.38PCh. 4 - Prob. 4.39PCh. 4 - Prob. 4.40APCh. 4 - Prob. 4.41APCh. 4 - Prob. 4.42APCh. 4 - Prob. 4.43APCh. 4 - Prob. 4.44APCh. 4 - Prob. 4.45APCh. 4 - Prob. 4.46APCh. 4 - Prob. 4.47APCh. 4 - Prob. 4.48APCh. 4 - Prob. 4.49APCh. 4 - Prob. 4.50APCh. 4 - Prob. 4.51APCh. 4 - Prob. 4.52APCh. 4 - Prob. 4.53APCh. 4 - Prob. 4.54APCh. 4 - Prob. 4.55APCh. 4 - Prob. 4.56APCh. 4 - Prob. 4.57APCh. 4 - Prob. 4.58APCh. 4 - Prob. 4.59APCh. 4 - Prob. 4.60APCh. 4 - Prob. 4.61APCh. 4 - Prob. 4.62APCh. 4 - Prob. 4.63APCh. 4 - Prob. 4.64APCh. 4 - Prob. 4.65APCh. 4 - Prob. 4.66APCh. 4 - Prob. 4.67APCh. 4 - Prob. 4.68APCh. 4 - Prob. 4.69APCh. 4 - Prob. 4.70AP
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- The proportion of O, C and H in the graphite oxide depends on the preparation method, as long as the most oxidant, the most graphite is destroyed and has less O. Is it correct?arrow_forwardWrite the complete common (not IUPAC) name of each molecule below. Note: if a molecule is one of a pair of enantiomers, be sure you start its name with D- or L- so we know which enantiomer it is. molecule C=O H3N CH3 common name (not the IUPAC name) H ☐ C=O H O-C-CH2-CH2 010 NH3 ☐ H3N ☐ HO 5arrow_forwardWrite the systematic name of each organic molecule: structure CI CH3 HO-C-CH-CH-CH2 – CH— CH3 CH3 name X O ☐ CH3-CH-CH2-CH2-C-OH CH3 11 HO-C-CH-CH2-OH CH3 ☐arrow_forward
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- Consider the following nucleophilic substitution reaction. The compound listed above the arrow is the solvent for the reaction. If nothing is listed over the arrow, then the nucleophile is also the solvent for the reaction. Part: 0/2 Part 1 of 2 Br acetone + I What is the correct mechanism for the reaction? Select the single best answer. OSN 1 OSN 2 X Part: 1/2 Part 2 of 2 Draw the products for the reaction. Include both the major organic product and the inorganic product. If more than one stereoisomer is possible, draw only one stereoisomer. Include stereochemistry where relevant. Click and drag to start drawing a structure. Х 5 ☐arrow_forwardTriethyloxonium tetrafluoroborate reacts with ethanol (CH3CH2OH) to give diethyl ether (CH3CH2OCH2CH3). BF triethyloxonium tetrafluoroborate Which equation, including the curved arrows, best represents the rate-determining step in the mechanism? Select the single best answer. O OH CH3CH2 OH + H. 0+ CH₂H₂ :0 + 0+ ж + H + :0: 0 Carrow_forwardCH3CH2CH=CH2 + H₂O − H+arrow_forward
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