Based on the reaction schemes below, what is the name of product D? OH Ja OH O A. 1-Methylcyclopropan-1-ol OB. Hydroxybenzene O D. Sodium phenolate O c. 1-Methylcycloprop-1-ene F. Methoxybenzene HC1 25 °C NaOH DMF O E. 1-Chloro-1-methylcyclopropane G. Methylenecyclopropane D A Mel NaOEt EtOH, 70 °C B BBr3 C HgSO4 H₂O, NaBH4 E (80%) + F (20%), G
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- Please help me answer the 4 pre lab questions (Determining the ethalpy of neutralization reactions)best condition for the reaction (1r,2s)-1 bromo-2methylcyclohexane->(s)3-methylcyclohex-1eneCompound X is insoluble in cold KMnO4, Br2 in CCl4, and conc. H2SO4. Compound X is most likely: a. an alkane b. none of these c. an alkene d. an alcohol e. an alkyl halide Indicate which of the ff. statements regarding nucleophilicity is incorrect. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. Second row elements are more nucleophilic than first row elements of comparable basicity. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon Which of the following alkynes can be deprotonated by NaNH2 in liquid NH3? 3-Methylhex-2-yne Pent-2-yne 3-Methylbutyne none of these Hex-3-yne
- Showusing expanded form the complete halogenation (using Br and UV light) of 2-butyne (2equations). Name your products after the first and second reaction.Predict the product of this reaction 1. 7-Bromo-3-octene + Cl2 2. 1-Cyclohexene + H2 3. 1-propene + HBr 4. 3-fluoro-2-methylpentane ---> _____ + HF (For Alkene and Alkyne Naming, follow this format “Branch-Carbon Prefix-Functional Group Suffix”) e.g. 3-methylhex-2-eneFill in necessary products reactants or reagants of these reactions. Please note the existence of enantionmers in some cases.
- Give all possible monosubstituted products for the reaction between propane and bromine in the presence of light. Determine the major product. I know the major product is 2-bromopopane but can I want to know if what im doing is right :) I used relative yieldPredict the product(s) OR reactants for the reactions by drawing the appropriate structure(s) in the boxes below. NOTE: Only draw ORGANIC products or reactants in the boxes and one compound per box. note: should be one major and 2 minor products for b.Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?