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Production drawings

Marking products has its limitations as it may damage the product, be removed, or deteriorate during subsequent processing. If applied directly to the product, the location and nature of identification should be specified in the product drawings or referenced process specifications. If applied to labels which themselves are permanently secured to the product, the identification needs to be visible when the product is installed so as to facilitate checks without its removal. [Pg.429]

Specify the status identification methods to be used in product drawings and specifications. [Pg.431]

The cleavage reaction occurs in three steps O protonation of the epoxide, Sn2 nucleophilic attack on the protonated epoxide, and deprotonation of the ring-opened product. Draw the complete mechanism. How many intermediates are there Which step determines diol stereochemistry ... [Pg.129]

Reaction of HBr with 3-methylcyc)ohexene yields a mixture of four products os- and trara-l-bromo-3-methylcyclohexane and cis- and fra/75-l-bromo-2-methylcyclohexane. The analogous reaction of HBr with 3-bromocyclohexene yields tra/TS-l,2-dibromocyclohexane as the sole product. Draw structures of the possible intermediates, and then explain wThy only a single product is formed in the reaction of HBr with 3-bromocvclohexene. [Pg.257]

Problem 16.1 Monobromination of toluene gives a mixture of three bromotoluene products. Draw and name them. [Pg.550]

These possible sources of problems in a molded part should be marked on the product drawing and explained to the mold designer for corrective action or creating an awareness of possible product defects. This is a necessary step in the chain of events in which the aim is to produce a tool that will provide useful products. Even if the mold s design, workmanship, and operation are carried out to the highest degree of quality, they cannot overcome a built-in weakness due to the product design. [Pg.183]

Exp lam and demonstrate clearly how spectroelectrochemistry can provide useful information about a reaction mechanism involving a redox process followed by a chemical reaction (EC mechanism), involving decomposition of the reaction product. Draw an absorbance-time plot for different rate constants of the decomposition reaction. [Pg.58]

Consider the elimination reaction below, which uses a strong, sterically hindered base (LDA). The product will be a double bond. This reaction will produce the Hoffmann product. Draw this product. [Pg.183]

Methylcyclohexene reacts with hydrogen chloride to form two products. Draw a... [Pg.64]

Clean fuels regulations in both the European and American markets have had a substantial impact on a refiner s ability to maximize product draws at the refinery front end. Extremely low sulfur requirements for... [Pg.328]

Administration of oral solution - A prazo am intensol is a concentrated oral solution. It is recommended that the oral solution be mixed with liquids or semi-solid food such as water, juices, soda or soda-like beverages, applesauce, and puddings. Use only the calibrated dropper provided with this product. Draw into the dropper the amount prescribed for a single dose. Then squeeze the dropper contents into a liquid or semi-solid food. Stir the liquid or food gently for a few seconds. The formulation blends quickly and completely. Consume the entire amount of the mixture of drug and liquid or drug and food immediately. Do not store for future use. [Pg.1014]

This intermediate is of course another, less stable, enolate anion, and in the ethanolic solution it will protonate to give the final product. Draw this. [Pg.111]

The outcome of the development stages are the final production drawings which are released to the manufacturing plant for production. An interim step is the ordering of tooling as soon as the production drawings are available to tool engineering. Once the tools and equipment are available to production, a tool and material tryout is conducted and any problems that may exist are corrected. [Pg.129]

N=C=S—OlOHsh]2 are produced, (t has been postulated that both remote and adjacent atiacks are involved in the formation of these products. Draw bridging intermediates consistent with this view for the formation of both products. ... [Pg.827]

From an operating standpoint, we can see when this flooding starts. As we decrease the pumparound duty, the temperature difference between the diesel- and gas-oil product draws should increase. When these two temperatures start to come together, we may assume that we have exceeded the incipient flood point, and that trays 5, 6, and 7 are beginning to flood. [Pg.145]

PROBLEM 23.18 The reaction of 2-pentene with H20 in the presence of H2S04 yields a mixture of two alcohol products. Draw their structures. [Pg.1004]

Step 7. Construct an orbital correlation diagram (Fig. 3.1). Following the assumption that an orbital in the starting material must feed into an orbital of the same symmetry in the product, draw lines connecting the orbitals of the starting materials to those of the products nearest in energy and of the same symmetry. Thus, y/x (S) connects to cr, (S), n (S) connects to n (S), and y/2 (A) connects to unoccupied orbitals, y/3 (S) connects to o, (A) connects to te (A), and (A) connects to (A). [Pg.36]

Accord Enterprise Informatics (AEI) products integrate to offer an Oracle-based enterprise-wide solution for chemical information management. These products draw on the power of the Accord Chemistry Engine and Oracle databases to store, search, and analyze chemical structures, related biological and chemical data, experimental results, and registration information. [Pg.53]

Consider how a nucleophilic site on another reactant (or, in a cyclization in another part of the same molecule) can attack the strong electrophile to form a bond needed in the product. Draw the product of this bond formation. [Pg.492]

If the combination of these two centres appears to lead to the product, draw the reactants, complete with charges, so as to position the nucleophilic and electrophilic centres within bonding distance ensuring that the angle of attack of the nucleophile is more or less consistent with the orbitals involved... [Pg.132]

Revision problem. The local anaesthetic proparacaine is made by this sequence of reactions. Deduce a structure for each product. Draw a mechanism for each step and explain why it gives that particular product. [Pg.578]

Problem 7.9 Draw the product of nucleophilic substitution with each neutral nucleophile. When the initial substitution product can lose a proton to form a neutral product, draw that product as well. [Pg.238]

When CH3CH2CH2CH2OH is treated with H2SO4 + NaBr, CH3CH2CH2CH2Br is the major product, and CH3CH2CH = CH2 and CH3CH2CH2CH2OCH2CH2CH2CH3 are isolated as minor products. Draw a mechanism that accounts for the... [Pg.356]

When acetaldehyde (CH3CHO) is treated with three equivalents of formaldehyde (CH2=O) in the presence of aqueous Na2C03, (H0CH2)3CCH0 is formed as product. Draw a stepwise mechanism for this process. [Pg.944]


See other pages where Production drawings is mentioned: [Pg.1331]    [Pg.343]    [Pg.348]    [Pg.93]    [Pg.279]    [Pg.428]    [Pg.218]    [Pg.1154]    [Pg.387]    [Pg.595]    [Pg.343]    [Pg.312]   
See also in sourсe #XX -- [ Pg.109 , Pg.148 ]




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