How might you syntheatce the following substances from Benzene ?. Please show the reagents and step necessary ? © 4- bromo - 1- notro-2-propyldentere
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- From cyclohexane and any other necessary reagentsDraw a structural formula for the major organic product of the reaction shown below. & CH₂ (oran CH3CH₂O -CuLi 2 ether You do not have to consider stereochemistry. Sn [F ? ChemDoodle H3O +3) Show how you would synthesize the following Compounds, storting with benzene or toluene ond ASSume any necessory pro duct (ond seperoble from ortho) in ortho, pora reogents, poro is the mogor mixture c)o- chlorobenzoic ocid d) m- chloronitro benzene
- Provide efficient syntheses of the following compounds using 1-pentene as your starting material and using any other necessary reagents. ? HO ?4) Which reagents and conditions should be used for the following reaction? OH O NABH4, CH3OH O CH3COCI, AICI3 O K2Cr207, H2SO4, H2O, heat OPCC, CH2C12 O1) LIAIH4, dry ether; 2) H2OWhich of the following is a ketone? А. (CH3)2Cнон В. СнзсоснЗ О с. снзсно D. CH3CH20CH3 What is the IUPAC nar e for the following structure? HO, a) cyclohexenol b) 3-cyclohexen-1-ol c) 1-cyclohexen-4-ol d) 4-cyclohexenol a How many Kekule structures are possible for naphthalene? A. 3 В. 4 С. 5 O D. 6
- CH3 CH3 CH3 CH;=ĊCH,CHCH;OH H2SO4, H3C H3C Referring to the above reaction: 1. Which atom does the H2SO4 first remove? 2. Identify the reaction if it's hydrogenation, hydrohalogenation, etc. 3. Propose a mechanism for the reaction, using the arrow formalism to indicate the flow of electrons.ua U LIIUUSE une correct name tor each structure shown. [ Select) H. CH3 [ Select ] a- OH O CH) HO-E-E- -CH,-CH, CH, [ Select ) V [ Select ] CH-CH,-CH2-C-o-CH, methyl butanoate methyl carboxybutane butyl methanoate CH,-CH-NH-CH, CH, methyl butyl ester H3CN-CH3 'N' [ Select ) [ Select ) H. CH3 -OH [ Select ] CI O CH, HO-C -CH,-CH, [ Select ) ČH, ( Select ) CH,-CH, -CH2-č-o-CH, CH,-CH-NH-CH, V[ Select ] CH, 1,1-dimethylbenzne dimethyl-nitro-benzene H3C CH3 N. 1,1 dimethylcyclohexane N-methyl-2-propanamine [ Sel [ Select ] CH3-CH2-CH2-c-o-CH, CH3-CH-NH-CH; ( Select ] ČH3 H3C., -CH V [ Select ] dimethyl-nitro-benzene 1,1 dimethylcyclohexane N,N - dimethylaniline 1,1-dimethylbenzne NH, [ Select) H,C. NH, [ Select ] CH3-CH2-C-NH - CH,How to synthesize 1-methylcyclohexene from cyclohexanone?
- Draw the structure of the products formed in the following reactions. a) CN H,0, H* CH3 он b) H3C- -CI + CH3 c) CH3 KMNO4, A, H,O" CH3 d) Br Mg, éther CO, H*Show how to prepare compound from 1-heptene. Q) 2-OctyneMelamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.