Classify each of the following as either a substitution, elimination, or addition reaction.дноOHH+H+ HO-+ Cl2+ H₂OCIΔDBU+ HCI+ HCIH*.OH+ HO+ H₂Ni / COHsubstitutioneliminationO additionsubstitutioneliminationO additionsubstitutioneliminationO additionsubstitutioneliminationadditionsubstitutioneliminationaddition

Step 1: Step 2: Step 3: Step 4:

Answered: Classify each of the following as…

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter37: The Aldol Condensation Reaction: Preparation Of Benzalacetophenones (chalcones)

Section: Chapter Questions

Problem 2Q

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In the reaction given below, what type of reaction is used? n-Pentane → Isopentane нннн H ITH Н—С—с—С—с —О —Н Н—с—с— с-с—н ||| | H нн H Addition Elimination Substitution Rearrangement
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Classify the following reaction as: addition, elimination, substitution, or rearrangement.
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Free radical halogenation is used to replace one or more hydrogens on an alkane with one or more halogens (either chlorine or bromine). It is a substitution reaction. A student performs a free radical bromination on 3-methyl-pentane (5.88 g) to create the desired product of 3-bromo-3-methyl-pentane. The product mix, which hopefully contains almost all 3-bromo-3-methyl-pentane, is cleaned up by passing it through a gas chromoatograph, which separates out the 3-bromo-3-methyl-pentane from any undesired products made during the reaction (undesired products are created frequently in free radical halogenation). The initial product mix weighed 9.45 g; the purified 3-bromo-3-methyl-pentane weighed 7.21 g. What is the student's percent recovery?
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PLS HELP ASAP ON ALL ASKED QUESTIONS PLS
Naming branched alkanes Name the following organic compounds: compound CH₁₂ | - - CH₂ — CH₂▬ CH₂ | CH - name CH3 血 - - - CH2 CH2 CH2 - - CH3 CH2 — CH₂ — C - - - - CH₂ — CH₂ — CH3 CH, CH₂ CH3 - CH | CH₂ - CH2- - П CH2-CH3 ☐
naming a chemical compound. I'm currently learning how to name alkanes and alkyl halides. Im confused about the compound ethanal, or acetaldehyde. The second carbon has a double bond on its hydrogen, so I'm wondering why the infix is "an" instead of "en". Frpm the table of infixes, it says "an" is for single bonds. Can someone help me understand

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