For the following reaction, list all expected organic and covalent products. This question does not require a mechanism, just the products. NANH2
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- The addition of water to aldehydes and ketones occurs rapidly, although it is not thermodynamically favored. What would be the product for the reaction above? Hint: Think of the self-ionization of water and the polarity of the carbonyl group.3) Draw the structures of the major organic product(s) for the following reactions. HI in CH₂Cl₂ 3 excess Cl₂ in H₂O H₂SO4 in H₂O (Two products) Br-Cl in THF 1) BH3 2) alkaline H₂O₂ OSO4 + HOOHA certain hydrocarbon had the molecular formula C16H26 and contained two triple bonds. Ozonolysis gave CH3(CH2), CO₂H and HO₂CCH2CH2CH2CH2CO₂H as the only products. Draw a reasonable structure for this hydrocarbon. Click and drag to start drawing a structure. D:
- Provide the systematic name for each of the following isomeric esters with the chemical formula C-H1202. (Be sure to indicate double bond stereochemistry using (E)/(Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) ball & stick labels ball & stick labels ball & stick + labelsThe conversion of alcohols into alkyl halides by reaction with hydrogen halides is an example of a Nucleophilic Substitution Reaction. This kind of reaction can proceed by two different mechanisms depending on the structure of alcohol substrates used. Generally, primary alcohols are substituted via SN2 mechanism, while secondary and tertiary alcohols undergo SN1 mechanism. Consider the following reaction given in the picture below and the questions in the picture too.田 [Review Topics] [References] Use the References to access important values if needed for this question. Draw the structure of the organic product of the following dehydration reaction. If more than one product is possible, draw the structure of the major product. H2S04 CH,CH2CH2CH2OH heat • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. P. opy aste [片 CH ChemDoodle Previous Next Save and Exit 10:23 AM Cengage Learning Cengage Technical Support へ首见口会 4/27/2021 Epic 江I 門 SUS
- МЕСНANISMS 1,2-epoxy-1-methylcyclopentane undergoes both acid-catalyzed and base-catalyzed opening of the epoxide ring to form two different products. > Using ethanol as the solvent and an appropriate acid, show the steps in the acid catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). > Using ethanol as the solvent and an appropriate base, show the steps in the base- catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). 1,2-epoxy-1-methylcyclopentane CH3(1) (2) The electrophilic addition of HBr to the alkene (3) gives rise to a bromoalkane product as shown in Figure 1. Draw the structure of the bromoalkane product. Draw the structure of the intermediate species leading to this product. • Identify which step of the reaction is the fast step and which is the slow step. Using the curly arrow notation draw a mechanism for this reaction. Step 1 Step 2 Н-Br [ Intermediate Species ] + Bromoalkane (3)3. It is required to introduce a halogen group to a five membered ring, thiophene. Discuss the reaction mechanism involved in the reaction by selecting a suitable halogen group and analyze why a particular substituted product obtained after the reaction is predominant over the other possible product(s) with the help of reactions. To meet the ever increasing demand of global population, the demand for textile products and consumption of dyes by these industries is increasing.
- Predict the major products of the following organic reaction: la ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers.3. Explain in terms of bonding why ethene mostly undergoes electrophilic addition reactions. Draw the mechanism for the reaction of but-1-ene and hydrogen bromide. Show, via the mechanisms that are two different possible isomers – explain which one is formed preferentially and why this occurs.A catalytic reduction of an alkene is shown below, what are all the possible products produced from this reaction. What is the relationship between the products? Is this a stereoselective, stereospecific reaction or neither? Explain. H2, Pd/C